Canonical Allele Identifier: CA2077138399
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188758G= , CM000675.2:g.20188758G= GRCh38
NC_000013.10:g.20762897G= , CM000675.1:g.20762897G= GRCh37
NC_000013.9:g.19660897G= NCBI36
NG_008358.1:g.9218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.*143C= ENSP00000372295.1:n.*143C=
ENST00000382848.5:c.*143C= MANE Select ENSP00000372299.4:n.*143C=
ENST00000382844.1:c.*143C= ENSP00000372295.1:n.*143C=
ENST00000382848.4:c.*143C= ENSP00000372299.4:n.*143C=
NM_004004.5:c.*143C= NP_003995.2:n.*143C=
XM_011535049.1:c.*143C= XP_011533351.1:n.*143C=
XM_011535049.2:c.*143C= XP_011533351.1:n.*143C=
NM_004004.6:c.*143C= MANE Select NP_003995.2:n.*143C=