Canonical Allele Identifier: CA2077114675
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20192789C= , CM000675.2:g.20192789C= GRCh38
NC_000013.10:g.20766928C= , CM000675.1:g.20766928C= GRCh37
NC_000013.9:g.19664928C= NCBI36
NG_008358.1:g.5187G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382848.5:c.-29G= MANE Select ENSP00000372299.4:n.-29G=
ENST00000382848.4:c.-29G= ENSP00000372299.4:n.-29G=
NM_004004.5:c.-29G= NP_003995.2:n.-29G=
NM_004004.6:c.-29G= MANE Select NP_003995.2:n.-29G=