Canonical Allele Identifier: CA2644769003

Linked Data

gnomAD v4: 1-34781680-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781680C>A , CM000663.2:g.34781680C>A GRCh38
NC_000001.10:g.35247281C>A , CM000663.1:g.35247281C>A GRCh37
NC_000001.9:g.35019868C>A NCBI36
NG_008309.1:g.5492C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-124C>A (GJB3) MANE Select ENSP00000362464.2:n.-124C>A
ENST00000373366.2:c.-124C>A (GJB3) ENSP00000362464.2:n.-124C>A
ENST00000426886.1:c.208-63271G>T (SMIM12) ENSP00000429902.1:n.208-63271G>T
NM_024009.2:c.-124C>A (GJB3) NP_076872.1:n.-124C>A
XR_947179.1:n.1001+16691G>T
XR_001737967.1:n.1023+16691G>T
NM_024009.3:c.-124C>A (GJB3) MANE Select NP_076872.1:n.-124C>A