Canonical Allele Identifier: CA483154291
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1530354
ClinVar RCV Id: RCV002089656
dbSNP Id: rs984555255
MyVariant Identifiers: chr13:g.20763124A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188985A>G , CM000675.2:g.20188985A>G GRCh38
NC_000013.10:g.20763124A>G , CM000675.1:g.20763124A>G GRCh37
NC_000013.9:g.19661124A>G NCBI36
NG_008358.1:g.8991T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.597T>C ENSP00000372295.1:p.Ser199=
ENST00000382848.5:c.597T>C MANE Select ENSP00000372299.4:p.Ser199=
ENST00000382844.1:c.597T>C ENSP00000372295.1:p.Ser199=
ENST00000382848.4:c.597T>C ENSP00000372299.4:p.Ser199=
NM_004004.5:c.597T>C NP_003995.2:p.Ser199=
XM_011535049.1:c.597T>C XP_011533351.1:p.Ser199=
XM_011535049.2:c.597T>C XP_011533351.1:p.Ser199=
NM_004004.6:c.597T>C MANE Select NP_003995.2:p.Ser199=