Canonical Allele Identifier: CA1143946911

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784850G= , CM000663.2:g.34784850G= GRCh38
NC_000001.10:g.35250451G= , CM000663.1:g.35250451G= GRCh37
NC_000001.9:g.35023038G= NCBI36
NG_008309.1:g.8662G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.88G= (GJB3) MANE Select ENSP00000362464.2:p.Val30=
ENST00000373362.3:c.88G= (GJB3) ENSP00000362460.3:p.Val30=
ENST00000373366.2:c.88G= (GJB3) ENSP00000362464.2:p.Val30=
ENST00000426886.1:c.208-66441C= (SMIM12) ENSP00000429902.1:n.208-66441C=
NM_001005752.1:c.88G= (GJB3) NP_001005752.1:p.Val30=
NM_024009.2:c.88G= (GJB3) NP_076872.1:p.Val30=
XR_947179.1:n.1001+13521C=
XR_001737967.1:n.1023+13521C=
NM_024009.3:c.88G= (GJB3) MANE Select NP_076872.1:p.Val30=
NM_001005752.2:c.88G= (GJB3) NP_001005752.1:p.Val30=