Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 6:112061098 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991252

Most severe consequence
Clinical significance

Synonyms

LSDB 11869

This variation has 18 HGVS names - click the plus to show

6:g.112061098C>A
ENST00000620524.1:c.156C>A
ENSP00000478049.1:p.Cys52Ter
ENST00000361714.3:c.156C>A
ENSP00000354734.2:p.Cys52Ter
ENST00000409166.3:c.-507-181C>A
ENST00000454589.3:c.156C>A
ENSP00000395928.1:p.Cys52Ter
ENST00000368663.3:c.90C>A
ENSP00000357652.3:p.Cys30Ter
ENST00000368664.5:c.210C>A
ENSP00000357653.3:p.Cys70Ter
ENST00000230529.7:c.156C>A
ENSP00000230529.5:p.Cys52Ter
ENST00000368666.4:c.210C>A
ENSP00000357655.3:p.Cys70Ter
ENST00000604763.3:c.156C>A
ENSP00000473777.1:p.Cys52Ter

Variation displays