Canonical Allele Identifier: CA1162033173

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784771G= , CM000663.2:g.34784771G= GRCh38
NC_000001.10:g.35250372G= , CM000663.1:g.35250372G= GRCh37
NC_000001.9:g.35022959G= NCBI36
NG_008309.1:g.8583G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.9G= (GJB3) MANE Select ENSP00000362464.2:p.Trp3=
ENST00000373362.3:c.9G= (GJB3) ENSP00000362460.3:p.Trp3=
ENST00000373366.2:c.9G= (GJB3) ENSP00000362464.2:p.Trp3=
ENST00000426886.1:c.208-66362C= (SMIM12) ENSP00000429902.1:n.208-66362C=
NM_001005752.1:c.9G= (GJB3) NP_001005752.1:p.Trp3=
NM_024009.2:c.9G= (GJB3) NP_076872.1:p.Trp3=
XR_947179.1:n.1001+13600C=
XR_001737967.1:n.1023+13600C=
NM_024009.3:c.9G= (GJB3) MANE Select NP_076872.1:p.Trp3=
NM_001005752.2:c.9G= (GJB3) NP_001005752.1:p.Trp3=