Canonical Allele Identifier: CA1140495598

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34784863T= , CM000663.2:g.34784863T= GRCh38
NC_000001.10:g.35250464T= , CM000663.1:g.35250464T= GRCh37
NC_000001.9:g.35023051T= NCBI36
NG_008309.1:g.8675T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.101T= (GJB3) MANE Select ENSP00000362464.2:p.Leu34=
ENST00000373362.3:c.101T= (GJB3) ENSP00000362460.3:p.Leu34=
ENST00000373366.2:c.101T= (GJB3) ENSP00000362464.2:p.Leu34=
ENST00000426886.1:c.208-66454A= (SMIM12) ENSP00000429902.1:n.208-66454A=
NM_001005752.1:c.101T= (GJB3) NP_001005752.1:p.Leu34=
NM_024009.2:c.101T= (GJB3) NP_076872.1:p.Leu34=
XR_947179.1:n.1001+13508A=
XR_001737967.1:n.1023+13508A=
NM_024009.3:c.101T= (GJB3) MANE Select NP_076872.1:p.Leu34=
NM_001005752.2:c.101T= (GJB3) NP_001005752.1:p.Leu34=