Canonical Allele Identifier: CA274369
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189092
dbSNP Id: rs786204690

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189174G>T , CM000675.2:g.20189174G>T GRCh38
NC_000013.10:g.20763313G>T , CM000675.1:g.20763313G>T GRCh37
NC_000013.9:g.19661313G>T NCBI36
NG_008358.1:g.8802C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.408C>A ENSP00000372295.1:p.Tyr136Ter
ENST00000382848.5:c.408C>A MANE Select ENSP00000372299.4:p.Tyr136Ter
ENST00000382844.1:c.408C>A ENSP00000372295.1:p.Tyr136Ter
ENST00000382848.4:c.408C>A ENSP00000372299.4:p.Tyr136Ter
NM_004004.5:c.408C>A NP_003995.2:p.Tyr136Ter
XM_011535049.1:c.408C>A XP_011533351.1:p.Tyr136Ter
XM_011535049.2:c.408C>A XP_011533351.1:p.Tyr136Ter
NM_004004.6:c.408C>A MANE Select NP_003995.2:p.Tyr136Ter