Canonical Allele Identifier: CA339310242

Linked Data

gnomAD v4: 1-34784776-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784776C>G , CM000663.2:g.34784776C>G GRCh38
NC_000001.10:g.35250377C>G , CM000663.1:g.35250377C>G GRCh37
NC_000001.9:g.35022964C>G NCBI36
NG_008309.1:g.8588C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.14C>G (GJB3) MANE Select ENSP00000362464.2:p.Thr5Arg
ENST00000373362.3:c.14C>G (GJB3) ENSP00000362460.3:p.Thr5Arg
ENST00000373366.2:c.14C>G (GJB3) ENSP00000362464.2:p.Thr5Arg
ENST00000426886.1:c.208-66367G>C (SMIM12) ENSP00000429902.1:n.208-66367G>C
NM_001005752.1:c.14C>G (GJB3) NP_001005752.1:p.Thr5Arg
NM_024009.2:c.14C>G (GJB3) NP_076872.1:p.Thr5Arg
XR_947179.1:n.1001+13595G>C
XR_001737967.1:n.1023+13595G>C
NM_024009.3:c.14C>G (GJB3) MANE Select NP_076872.1:p.Thr5Arg
NM_001005752.2:c.14C>G (GJB3) NP_001005752.1:p.Thr5Arg