Canonical Allele Identifier: CA916083191
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869299
ClinVar RCV Id: RCV001078358
dbSNP Id: rs1847555115

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226649del , CM000673.2:g.5226649del GRCh38
NC_000011.9:g.5247879del , CM000673.1:g.5247879del GRCh37
NC_000011.8:g.5204455del NCBI36
NG_000007.3:g.70968del
NG_059281.1:g.5424del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.244del ENSP00000494175.1:p.Leu82SerfsTer8
ENST00000335295.4:c.244del MANE Select ENSP00000333994.3:p.Leu82SerfsTer8
ENST00000380315.2:c.244del ENSP00000369671.2:p.Leu82SerfsTer8
ENST00000475226.1:n.176del
ENST00000485743.1:n.295del
ENST00000633227.1:c.*60del ENSP00000488004.1:n.*60del
NM_000518.4:c.244del NP_000509.1:p.Leu82SerfsTer8
NM_000518.5:c.244del MANE Select NP_000509.1:p.Leu82SerfsTer8