Canonical Allele Identifier: CA339313667

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34785148G>A , CM000663.2:g.34785148G>A GRCh38
NC_000001.10:g.35250749G>A , CM000663.1:g.35250749G>A GRCh37
NC_000001.9:g.35023336G>A NCBI36
NG_008309.1:g.8960G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.386G>A (GJB3) MANE Select ENSP00000362464.2:p.Trp129Ter
ENST00000373362.3:c.386G>A (GJB3) ENSP00000362460.3:p.Trp129Ter
ENST00000373366.2:c.386G>A (GJB3) ENSP00000362464.2:p.Trp129Ter
ENST00000426886.1:c.208-66739C>T (SMIM12) ENSP00000429902.1:n.208-66739C>T
NM_001005752.1:c.386G>A (GJB3) NP_001005752.1:p.Trp129Ter
NM_024009.2:c.386G>A (GJB3) NP_076872.1:p.Trp129Ter
XR_947179.1:n.1001+13223C>T
XR_001737967.1:n.1023+13223C>T
NM_024009.3:c.386G>A (GJB3) MANE Select NP_076872.1:p.Trp129Ter
NM_001005752.2:c.386G>A (GJB3) NP_001005752.1:p.Trp129Ter