Canonical Allele Identifier: CA658823443
Gene: GJB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 550390
ClinVar RCV Id: RCV000665123
dbSNP Id: rs1555341783

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188913_20188916del , CM000675.2:g.20188913_20188916del GRCh38
NC_000013.10:g.20763052_20763055del , CM000675.1:g.20763052_20763055del GRCh37
NC_000013.9:g.19661052_19661055del NCBI36
NG_008358.1:g.9062_9065del

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.668_671del ENSP00000372295.1:p.Lys223SerfsTer10
ENST00000382848.5:c.668_671del MANE Select ENSP00000372299.4:p.Lys223SerfsTer10
ENST00000382844.1:c.668_671del ENSP00000372295.1:p.Lys223SerfsTer10
ENST00000382848.4:c.668_671del ENSP00000372299.4:p.Lys223SerfsTer10
NM_004004.5:c.668_671del NP_003995.2:p.Lys223SerfsTer10
XM_011535049.1:c.668_671del XP_011533351.1:p.Lys223SerfsTer10
XM_011535049.2:c.668_671del XP_011533351.1:p.Lys223SerfsTer10
NM_004004.6:c.668_671del MANE Select NP_003995.2:p.Lys223SerfsTer10