Canonical Allele Identifier: CA10611067

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34785806G>A , CM000663.2:g.34785806G>A GRCh38
NC_000001.10:g.35251407G>A , CM000663.1:g.35251407G>A GRCh37
NC_000001.9:g.35023994G>A NCBI36
NG_008309.1:g.9618G>A

Transcript Alleles

HGVS Amino-acid Change
NM_024009.3:c.*231G>A (GJB3) MANE Select NP_076872.1:n.*231G>A
ENST00000373366.3:c.*231G>A (GJB3) MANE Select ENSP00000362464.2:n.*231G>A
NM_001005752.1:c.*231G>A (GJB3) NP_001005752.1:n.*231G>A
NM_001005752.2:c.*231G>A (GJB3) NP_001005752.1:n.*231G>A
NM_024009.2:c.*231G>A (GJB3) NP_076872.1:n.*231G>A
ENST00000373362.3:c.*231G>A (GJB3) ENSP00000362460.3:n.*231G>A
ENST00000373366.2:c.*231G>A (GJB3) ENSP00000362464.2:n.*231G>A
ENST00000426886.1:c.208-67397C>T (SMIM12) ENSP00000429902.1:n.208-67397C>T
XR_001737967.1:n.1023+12565C>T
XR_947179.1:n.1001+12565C>T