Canonical Allele Identifier: CA339310456

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784808T>G , CM000663.2:g.34784808T>G GRCh38
NC_000001.10:g.35250409T>G , CM000663.1:g.35250409T>G GRCh37
NC_000001.9:g.35022996T>G NCBI36
NG_008309.1:g.8620T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.46T>G (GJB3) MANE Select ENSP00000362464.2:p.Tyr16Asp
ENST00000373362.3:c.46T>G (GJB3) ENSP00000362460.3:p.Tyr16Asp
ENST00000373366.2:c.46T>G (GJB3) ENSP00000362464.2:p.Tyr16Asp
ENST00000426886.1:c.208-66399A>C (SMIM12) ENSP00000429902.1:n.208-66399A>C
NM_001005752.1:c.46T>G (GJB3) NP_001005752.1:p.Tyr16Asp
NM_024009.2:c.46T>G (GJB3) NP_076872.1:p.Tyr16Asp
XR_947179.1:n.1001+13563A>C
XR_001737967.1:n.1023+13563A>C
NM_024009.3:c.46T>G (GJB3) MANE Select NP_076872.1:p.Tyr16Asp
NM_001005752.2:c.46T>G (GJB3) NP_001005752.1:p.Tyr16Asp