Canonical Allele Identifier: CA339310474

Linked Data

dbSNP Id: rs1272680545
gnomAD v3: 1-34784812-C-A
gnomAD v4: 1-34784812-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784812C>A , CM000663.2:g.34784812C>A GRCh38
NC_000001.10:g.35250413C>A , CM000663.1:g.35250413C>A GRCh37
NC_000001.9:g.35023000C>A NCBI36
NG_008309.1:g.8624C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.50C>A (GJB3) MANE Select ENSP00000362464.2:p.Ser17Tyr
ENST00000373362.3:c.50C>A (GJB3) ENSP00000362460.3:p.Ser17Tyr
ENST00000373366.2:c.50C>A (GJB3) ENSP00000362464.2:p.Ser17Tyr
ENST00000426886.1:c.208-66403G>T (SMIM12) ENSP00000429902.1:n.208-66403G>T
NM_001005752.1:c.50C>A (GJB3) NP_001005752.1:p.Ser17Tyr
NM_024009.2:c.50C>A (GJB3) NP_076872.1:p.Ser17Tyr
XR_947179.1:n.1001+13559G>T
XR_001737967.1:n.1023+13559G>T
NM_024009.3:c.50C>A (GJB3) MANE Select NP_076872.1:p.Ser17Tyr
NM_001005752.2:c.50C>A (GJB3) NP_001005752.1:p.Ser17Tyr