Canonical Allele Identifier: CA2077110238
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189612G= , CM000675.2:g.20189612G= GRCh38
NC_000013.10:g.20763751G= , CM000675.1:g.20763751G= GRCh37
NC_000013.9:g.19661751G= NCBI36
NG_008358.1:g.8364C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.-31C= ENSP00000372295.1:n.-31C=
ENST00000382848.5:c.-22-9C= MANE Select ENSP00000372299.4:n.-22-9C=
ENST00000382844.1:c.-31C= ENSP00000372295.1:n.-31C=
ENST00000382848.4:c.-22-9C= ENSP00000372299.4:n.-22-9C=
NM_004004.5:c.-22-9C= NP_003995.2:n.-22-9C=
XM_011535049.1:c.-22-9C= XP_011533351.1:n.-22-9C=
XM_011535049.2:c.-22-9C= XP_011533351.1:n.-22-9C=
NM_004004.6:c.-22-9C= MANE Select NP_003995.2:n.-22-9C=