Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 3:165830567 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970162

Most severe consequence
Clinical significance

Synonyms

LSDB 5076

This variation has 9 HGVS names - click the plus to show

3:g.165830567T>C
ENST00000482958.1:c.467A>G
ENSP00000419804.1:p.Tyr156Cys
ENST00000264381.4:c.467A>G
ENSP00000264381.3:p.Tyr156Cys
ENST00000479451.2:c.107+6747A>G
ENST00000488954.1:c.107+6747A>G
ENST00000497011.2:c.467A>G
ENSP00000419505.1:p.Tyr156Cys

Variation displays