Canonical Allele Identifier: CA217115218
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869360
ClinVar RCV Id: RCV001078432
dbSNP Id: rs281864898

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226949_5226955del , CM000673.2:g.5226949_5226955del GRCh38
NC_000011.9:g.5248179_5248185del , CM000673.1:g.5248179_5248185del GRCh37
NC_000011.8:g.5204755_5204761del NCBI36
NG_000007.3:g.70662_70668del
NG_059281.1:g.5118_5124del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.68_74del ENSP00000494175.1:p.Glu23ValfsTer?
ENST00000335295.4:c.68_74del MANE Select ENSP00000333994.3:p.Glu23ValfsTer?
ENST00000380315.2:c.68_74del ENSP00000369671.2:p.Glu23ValfsTer?
ENST00000485743.1:n.119_125del
ENST00000633227.1:c.68_74del ENSP00000488004.1:p.Glu23ValfsTer14
NM_000518.4:c.68_74del NP_000509.1:p.Glu23ValfsTer?
NM_000518.5:c.68_74del MANE Select NP_000509.1:p.Glu23ValfsTer?