Canonical Allele Identifier: CA1000465569

Linked Data

dbSNP Id: rs1057515515
gnomAD v3: 1-34781711-C-A
gnomAD v4: 1-34781711-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781711C>A , CM000663.2:g.34781711C>A GRCh38
NC_000001.10:g.35247312C>A , CM000663.1:g.35247312C>A GRCh37
NC_000001.9:g.35019899C>A NCBI36
NG_008309.1:g.5523C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-93C>A (GJB3) MANE Select ENSP00000362464.2:n.-93C>A
ENST00000373366.2:c.-93C>A (GJB3) ENSP00000362464.2:n.-93C>A
ENST00000426886.1:c.208-63302G>T (SMIM12) ENSP00000429902.1:n.208-63302G>T
NM_024009.2:c.-93C>A (GJB3) NP_076872.1:n.-93C>A
XR_947179.1:n.1001+16660G>T
XR_001737967.1:n.1023+16660G>T
NM_024009.3:c.-93C>A (GJB3) MANE Select NP_076872.1:n.-93C>A