Canonical Allele Identifier: CA2077138917
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189039A= , CM000675.2:g.20189039A= GRCh38
NC_000013.10:g.20763178A= , CM000675.1:g.20763178A= GRCh37
NC_000013.9:g.19661178A= NCBI36
NG_008358.1:g.8937T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.543T= ENSP00000372295.1:p.Phe181=
ENST00000382848.5:c.543T= MANE Select ENSP00000372299.4:p.Phe181=
ENST00000382844.1:c.543T= ENSP00000372295.1:p.Phe181=
ENST00000382848.4:c.543T= ENSP00000372299.4:p.Phe181=
NM_004004.5:c.543T= NP_003995.2:p.Phe181=
XM_011535049.1:c.543T= XP_011533351.1:p.Phe181=
XM_011535049.2:c.543T= XP_011533351.1:p.Phe181=
NM_004004.6:c.543T= MANE Select NP_003995.2:p.Phe181=