Canonical Allele Identifier: CA2077140012
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189382T= , CM000675.2:g.20189382T= GRCh38
NC_000013.10:g.20763521T= , CM000675.1:g.20763521T= GRCh37
NC_000013.9:g.19661521T= NCBI36
NG_008358.1:g.8594A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382844.2:c.200A= ENSP00000372295.1:p.His67=
ENST00000382848.5:c.200A= MANE Select ENSP00000372299.4:p.His67=
ENST00000382844.1:c.200A= ENSP00000372295.1:p.His67=
ENST00000382848.4:c.200A= ENSP00000372299.4:p.His67=
NM_004004.5:c.200A= NP_003995.2:p.His67=
XM_011535049.1:c.200A= XP_011533351.1:p.His67=
XM_011535049.2:c.200A= XP_011533351.1:p.His67=
NM_004004.6:c.200A= MANE Select NP_003995.2:p.His67=