Canonical Allele Identifier: CA1162031871

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34781632G= , CM000663.2:g.34781632G= GRCh38
NC_000001.10:g.35247233G= , CM000663.1:g.35247233G= GRCh37
NC_000001.9:g.35019820G= NCBI36
NG_008309.1:g.5444G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373366.3:c.-172G= (GJB3) MANE Select ENSP00000362464.2:n.-172G=
ENST00000373366.2:c.-172G= (GJB3) ENSP00000362464.2:n.-172G=
ENST00000426886.1:c.208-63223C= (SMIM12) ENSP00000429902.1:n.208-63223C=
NM_024009.2:c.-172G= (GJB3) NP_076872.1:n.-172G=
XR_947179.1:n.1001+16739C=
XR_001737967.1:n.1023+16739C=
NM_024009.3:c.-172G= (GJB3) MANE Select NP_076872.1:n.-172G=