Canonical Allele Identifier: CA2573149176
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1454400
ClinVar RCV Id: RCV001941854
dbSNP Id: rs2137307021

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188958del , CM000675.2:g.20188958del GRCh38
NC_000013.10:g.20763097del , CM000675.1:g.20763097del GRCh37
NC_000013.9:g.19661097del NCBI36
NG_008358.1:g.9018del

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.624del ENSP00000372295.1:p.Glu209AsnfsTer6
ENST00000382848.5:c.624del MANE Select ENSP00000372299.4:p.Glu209AsnfsTer6
ENST00000382844.1:c.624del ENSP00000372295.1:p.Glu209AsnfsTer6
ENST00000382848.4:c.624del ENSP00000372299.4:p.Glu209AsnfsTer6
NM_004004.5:c.624del NP_003995.2:p.Glu209AsnfsTer6
XM_011535049.1:c.624del XP_011533351.1:p.Glu209AsnfsTer6
XM_011535049.2:c.624del XP_011533351.1:p.Glu209AsnfsTer6
NM_004004.6:c.624del MANE Select NP_003995.2:p.Glu209AsnfsTer6