Canonical Allele Identifier: CA913190238
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 632845
dbSNP Id: rs35395625

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226718del , CM000673.2:g.5226718del GRCh38
NC_000011.9:g.5247948del , CM000673.1:g.5247948del GRCh37
NC_000011.8:g.5204524del NCBI36
NG_000007.3:g.70900del
NG_059281.1:g.5356del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.176del ENSP00000494175.1:p.Pro59LeufsTer3
ENST00000335295.4:c.176del MANE Select ENSP00000333994.3:p.Pro59LeufsTer3
ENST00000380315.2:c.176del ENSP00000369671.2:p.Pro59LeufsTer3
ENST00000475226.1:n.108del
ENST00000485743.1:n.227del
ENST00000633227.1:c.160del ENSP00000488004.1:p.Leu54Ter
NM_000518.4:c.176del NP_000509.1:p.Pro59LeufsTer3
NM_000518.5:c.176del MANE Select NP_000509.1:p.Pro59LeufsTer3