Canonical Allele Identifier: CA261641
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44728
dbSNP Id: rs111033451

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189563G>A , CM000675.2:g.20189563G>A GRCh38
NC_000013.10:g.20763702G>A , CM000675.1:g.20763702G>A GRCh37
NC_000013.9:g.19661702G>A NCBI36
NG_008358.1:g.8413C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.19C>T ENSP00000372295.1:p.Gln7Ter
ENST00000382848.5:c.19C>T MANE Select ENSP00000372299.4:p.Gln7Ter
ENST00000382844.1:c.19C>T ENSP00000372295.1:p.Gln7Ter
ENST00000382848.4:c.19C>T ENSP00000372299.4:p.Gln7Ter
NM_004004.5:c.19C>T NP_003995.2:p.Gln7Ter
XM_011535049.1:c.19C>T XP_011533351.1:p.Gln7Ter
XM_011535049.2:c.19C>T XP_011533351.1:p.Gln7Ter
NM_004004.6:c.19C>T MANE Select NP_003995.2:p.Gln7Ter