Canonical Allele Identifier: CA2077139547
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189265A= , CM000675.2:g.20189265A= GRCh38
NC_000013.10:g.20763404A= , CM000675.1:g.20763404A= GRCh37
NC_000013.9:g.19661404A= NCBI36
NG_008358.1:g.8711T=

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.317T= ENSP00000372295.1:p.Phe106=
ENST00000382848.5:c.317T= MANE Select ENSP00000372299.4:p.Phe106=
ENST00000382844.1:c.317T= ENSP00000372295.1:p.Phe106=
ENST00000382848.4:c.317T= ENSP00000372299.4:p.Phe106=
NM_004004.5:c.317T= NP_003995.2:p.Phe106=
XM_011535049.1:c.317T= XP_011533351.1:p.Phe106=
XM_011535049.2:c.317T= XP_011533351.1:p.Phe106=
NM_004004.6:c.317T= MANE Select NP_003995.2:p.Phe106=