Canonical Allele Identifier: CA387461563
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1067767
ClinVar RCV Id: RCV001379119
dbSNP Id: rs199883710

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189344G>T , CM000675.2:g.20189344G>T GRCh38
NC_000013.10:g.20763483G>T , CM000675.1:g.20763483G>T GRCh37
NC_000013.9:g.19661483G>T NCBI36
NG_008358.1:g.8632C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.238C>A ENSP00000372295.1:p.Gln80Lys
ENST00000382848.5:c.238C>A MANE Select ENSP00000372299.4:p.Gln80Lys
ENST00000382844.1:c.238C>A ENSP00000372295.1:p.Gln80Lys
ENST00000382848.4:c.238C>A ENSP00000372299.4:p.Gln80Lys
NM_004004.5:c.238C>A NP_003995.2:p.Gln80Lys
XM_011535049.1:c.238C>A XP_011533351.1:p.Gln80Lys
XM_011535049.2:c.238C>A XP_011533351.1:p.Gln80Lys
NM_004004.6:c.238C>A MANE Select NP_003995.2:p.Gln80Lys