Canonical Allele Identifier: CA677552557
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 993075
ClinVar RCV Id: RCV001283994
dbSNP Id: rs1489533338

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225836_5225846del , CM000673.2:g.5225836_5225846del GRCh38
NC_000011.9:g.5247066_5247076del , CM000673.1:g.5247066_5247076del GRCh37
NC_000011.8:g.5203642_5203652del NCBI36
NG_000007.3:g.71777_71787del
NG_059281.1:g.6233_6243del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.316-113_316-103del ENSP00000494175.1:n.316-113_316-103del
ENST00000335295.4:c.316-113_316-103del MANE Select ENSP00000333994.3:n.316-113_316-103del
ENST00000475226.1:n.248-113_248-103del
ENST00000633227.1:c.*132-113_*132-103del ENSP00000488004.1:n.*132-113_*132-103del
NM_000518.4:c.316-113_316-103del NP_000509.1:n.316-113_316-103del
NM_000518.5:c.316-113_316-103del MANE Select NP_000509.1:n.316-113_316-103del