Canonical Allele Identifier: CA916083209
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869244
ClinVar RCV Id: RCV001078279
dbSNP Id: rs1847579861

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226931del , CM000673.2:g.5226931del GRCh38
NC_000011.9:g.5248161del , CM000673.1:g.5248161del GRCh37
NC_000011.8:g.5204737del NCBI36
NG_000007.3:g.70685del
NG_059281.1:g.5141del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.91del ENSP00000494175.1:p.Arg31GlyfsTer?
ENST00000335295.4:c.91del MANE Select ENSP00000333994.3:p.Arg31GlyfsTer?
ENST00000380315.2:c.91del ENSP00000369671.2:p.Arg31GlyfsTer?
ENST00000485743.1:n.142del
ENST00000633227.1:c.76+15del ENSP00000488004.1:n.76+15del
NM_000518.4:c.91del NP_000509.1:p.Arg31GlyfsTer?
NM_000518.5:c.91del MANE Select NP_000509.1:p.Arg31GlyfsTer?