Canonical Allele Identifier: CA2077114465
Gene: GJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20192686T= , CM000675.2:g.20192686T= GRCh38
NC_000013.10:g.20766825T= , CM000675.1:g.20766825T= GRCh37
NC_000013.9:g.19664825T= NCBI36
NG_008358.1:g.5290A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382848.5:c.-23+97A= MANE Select ENSP00000372299.4:n.-23+97A=
ENST00000382848.4:c.-23+97A= ENSP00000372299.4:n.-23+97A=
NM_004004.5:c.-23+97A= NP_003995.2:n.-23+97A=
NM_004004.6:c.-23+97A= MANE Select NP_003995.2:n.-23+97A=