Canonical Allele Identifier: CA754881
Community Standard Title: NM_024009.3(GJB3):c.667C>A (p.Pro223Thr)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34785429C>A , CM000663.2:g.34785429C>A GRCh38
NC_000001.10:g.35251030C>A , CM000663.1:g.35251030C>A GRCh37
NC_000001.9:g.35023617C>A NCBI36
NG_008309.1:g.9241C>A

Transcript Alleles

HGVS Amino-acid Change
NM_024009.3:c.667C>A (GJB3) MANE Select NP_076872.1:p.Pro223Thr
ENST00000373366.3:c.667C>A (GJB3) MANE Select ENSP00000362464.2:p.Pro223Thr
NM_001005752.1:c.667C>A (GJB3) NP_001005752.1:p.Pro223Thr
NM_001005752.2:c.667C>A (GJB3) NP_001005752.1:p.Pro223Thr
NM_024009.2:c.667C>A (GJB3) NP_076872.1:p.Pro223Thr
ENST00000373362.3:c.667C>A (GJB3) ENSP00000362460.3:p.Pro223Thr
ENST00000373366.2:c.667C>A (GJB3) ENSP00000362464.2:p.Pro223Thr
ENST00000426886.1:c.208-67020G>T (SMIM12) ENSP00000429902.1:n.208-67020G>T
XR_001737967.1:n.1023+12942G>T
XR_947179.1:n.1001+12942G>T