Canonical Allele Identifier: CA339310376

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784797G>C , CM000663.2:g.34784797G>C GRCh38
NC_000001.10:g.35250398G>C , CM000663.1:g.35250398G>C GRCh37
NC_000001.9:g.35022985G>C NCBI36
NG_008309.1:g.8609G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.35G>C (GJB3) MANE Select ENSP00000362464.2:p.Gly12Ala
ENST00000373362.3:c.35G>C (GJB3) ENSP00000362460.3:p.Gly12Ala
ENST00000373366.2:c.35G>C (GJB3) ENSP00000362464.2:p.Gly12Ala
ENST00000426886.1:c.208-66388C>G (SMIM12) ENSP00000429902.1:n.208-66388C>G
NM_001005752.1:c.35G>C (GJB3) NP_001005752.1:p.Gly12Ala
NM_024009.2:c.35G>C (GJB3) NP_076872.1:p.Gly12Ala
XR_947179.1:n.1001+13574C>G
XR_001737967.1:n.1023+13574C>G
NM_024009.3:c.35G>C (GJB3) MANE Select NP_076872.1:p.Gly12Ala
NM_001005752.2:c.35G>C (GJB3) NP_001005752.1:p.Gly12Ala