Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 6:112064842 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991254

Most severe consequence
Clinical significance

Synonyms

LSDB 11867

This variation has 19 HGVS names - click the plus to show

6:g.112064842G>A
ENST00000361714.2:c.434G>A
ENSP00000354734.2:p.Cys145Tyr
ENST00000620524.1:c.434G>A
ENSP00000478049.1:p.Cys145Tyr
ENST00000409166.2:c.-303G>A
ENST00000454589.2:c.434G>A
ENSP00000395928.1:p.Cys145Tyr
ENST00000368663.3:c.365G>A
ENSP00000357652.3:p.Cys122Tyr
ENST00000613648.1:n.205G>A
ENST00000368664.4:c.488G>A
ENSP00000357653.3:p.Cys163Tyr
ENST00000230529.6:c.434G>A
ENSP00000230529.5:p.Cys145Tyr
ENST00000368666.3:c.488G>A
ENSP00000357655.3:p.Cys163Tyr
ENST00000604763.2:c.434G>A
ENSP00000473777.1:p.Cys145Tyr

Variation displays