Canonical Allele Identifier: CA2077138716
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188973G= , CM000675.2:g.20188973G= GRCh38
NC_000013.10:g.20763112G= , CM000675.1:g.20763112G= GRCh37
NC_000013.9:g.19661112G= NCBI36
NG_008358.1:g.9003C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.609C= ENSP00000372295.1:p.Ile203=
ENST00000382848.5:c.609C= MANE Select ENSP00000372299.4:p.Ile203=
ENST00000382844.1:c.609C= ENSP00000372295.1:p.Ile203=
ENST00000382848.4:c.609C= ENSP00000372299.4:p.Ile203=
NM_004004.5:c.609C= NP_003995.2:p.Ile203=
XM_011535049.1:c.609C= XP_011533351.1:p.Ile203=
XM_011535049.2:c.609C= XP_011533351.1:p.Ile203=
NM_004004.6:c.609C= MANE Select NP_003995.2:p.Ile203=