Canonical Allele Identifier: CA2077110347
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189642C= , CM000675.2:g.20189642C= GRCh38
NC_000013.10:g.20763781C= , CM000675.1:g.20763781C= GRCh37
NC_000013.9:g.19661781C= NCBI36
NG_008358.1:g.8334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.-61G= ENSP00000372295.1:n.-61G=
ENST00000382848.5:c.-22-39G= MANE Select ENSP00000372299.4:n.-22-39G=
ENST00000382844.1:c.-61G= ENSP00000372295.1:n.-61G=
ENST00000382848.4:c.-22-39G= ENSP00000372299.4:n.-22-39G=
NM_004004.5:c.-22-39G= NP_003995.2:n.-22-39G=
XM_011535049.1:c.-22-39G= XP_011533351.1:n.-22-39G=
XM_011535049.2:c.-22-39G= XP_011533351.1:n.-22-39G=
NM_004004.6:c.-22-39G= MANE Select NP_003995.2:n.-22-39G=