Canonical Allele Identifier: CA6904211
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 795789
dbSNP Id: rs563151740

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188907T>A , CM000675.2:g.20188907T>A GRCh38
NC_000013.10:g.20763046T>A , CM000675.1:g.20763046T>A GRCh37
NC_000013.9:g.19661046T>A NCBI36
NG_008358.1:g.9069A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.675A>T ENSP00000372295.1:p.Pro225=
ENST00000382848.5:c.675A>T MANE Select ENSP00000372299.4:p.Pro225=
ENST00000382844.1:c.675A>T ENSP00000372295.1:p.Pro225=
ENST00000382848.4:c.675A>T ENSP00000372299.4:p.Pro225=
NM_004004.5:c.675A>T NP_003995.2:p.Pro225=
XM_011535049.1:c.675A>T XP_011533351.1:p.Pro225=
XM_011535049.2:c.675A>T XP_011533351.1:p.Pro225=
NM_004004.6:c.675A>T MANE Select NP_003995.2:p.Pro225=