Canonical Allele Identifier: CA2077138762
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188986G= , CM000675.2:g.20188986G= GRCh38
NC_000013.10:g.20763125G= , CM000675.1:g.20763125G= GRCh37
NC_000013.9:g.19661125G= NCBI36
NG_008358.1:g.8990C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.596C= ENSP00000372295.1:p.Ser199=
ENST00000382848.5:c.596C= MANE Select ENSP00000372299.4:p.Ser199=
ENST00000382844.1:c.596C= ENSP00000372295.1:p.Ser199=
ENST00000382848.4:c.596C= ENSP00000372299.4:p.Ser199=
NM_004004.5:c.596C= NP_003995.2:p.Ser199=
XM_011535049.1:c.596C= XP_011533351.1:p.Ser199=
XM_011535049.2:c.596C= XP_011533351.1:p.Ser199=
NM_004004.6:c.596C= MANE Select NP_003995.2:p.Ser199=