Canonical Allele Identifier: CA6904295
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1943335
ClinVar RCV Id: RCV002650398
dbSNP Id: rs754237172

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189318C>G , CM000675.2:g.20189318C>G GRCh38
NC_000013.10:g.20763457C>G , CM000675.1:g.20763457C>G GRCh37
NC_000013.9:g.19661457C>G NCBI36
NG_008358.1:g.8658G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.264G>C ENSP00000372295.1:p.Ala88=
ENST00000382848.5:c.264G>C MANE Select ENSP00000372299.4:p.Ala88=
ENST00000382844.1:c.264G>C ENSP00000372295.1:p.Ala88=
ENST00000382848.4:c.264G>C ENSP00000372299.4:p.Ala88=
NM_004004.5:c.264G>C NP_003995.2:p.Ala88=
XM_011535049.1:c.264G>C XP_011533351.1:p.Ala88=
XM_011535049.2:c.264G>C XP_011533351.1:p.Ala88=
NM_004004.6:c.264G>C MANE Select NP_003995.2:p.Ala88=