Canonical Allele Identifier: CA2077110487
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189757A= , CM000675.2:g.20189757A= GRCh38
NC_000013.10:g.20763896A= , CM000675.1:g.20763896A= GRCh37
NC_000013.9:g.19661896A= NCBI36
NG_008358.1:g.8219T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.-176T= ENSP00000372295.1:n.-176T=
ENST00000382848.5:c.-22-154T= MANE Select ENSP00000372299.4:n.-22-154T=
ENST00000382844.1:c.-176T= ENSP00000372295.1:n.-176T=
ENST00000382848.4:c.-22-154T= ENSP00000372299.4:n.-22-154T=
NM_004004.5:c.-22-154T= NP_003995.2:n.-22-154T=
XM_011535049.1:c.-22-154T= XP_011533351.1:n.-22-154T=
XM_011535049.2:c.-22-154T= XP_011533351.1:n.-22-154T=
NM_004004.6:c.-22-154T= MANE Select NP_003995.2:n.-22-154T=