Canonical Allele Identifier: CA916083198
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869346
ClinVar RCV Id: RCV001078416
dbSNP Id: rs1847559573

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226716_5226728del , CM000673.2:g.5226716_5226728del GRCh38
NC_000011.9:g.5247946_5247958del , CM000673.1:g.5247946_5247958del GRCh37
NC_000011.8:g.5204522_5204534del NCBI36
NG_000007.3:g.70889_70901del
NG_059281.1:g.5345_5357del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.165_177del ENSP00000494175.1:p.Met56ArgfsTer2
ENST00000335295.4:c.165_177del MANE Select ENSP00000333994.3:p.Met56ArgfsTer2
ENST00000380315.2:c.165_177del ENSP00000369671.2:p.Met56ArgfsTer2
ENST00000475226.1:n.97_109del
ENST00000485743.1:n.216_228del
ENST00000633227.1:c.149_161del ENSP00000488004.1:p.Leu50Ter
NM_000518.4:c.165_177del NP_000509.1:p.Met56ArgfsTer2
NM_000518.5:c.165_177del MANE Select NP_000509.1:p.Met56ArgfsTer2