Canonical Allele Identifier: CA891862903
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 590977
ClinVar RCV Id: RCV000722147
dbSNP Id: rs1564875331

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226724_5226728delinsTGATGCC , CM000673.2:g.5226724_5226728delinsTGATGCC GRCh38
NC_000011.9:g.5247954_5247958delinsTGATGCC , CM000673.1:g.5247954_5247958delinsTGATGCC GRCh37
NC_000011.8:g.5204530_5204534delinsTGATGCC NCBI36
NG_000007.3:g.70888_70892delinsGGCATCA
NG_059281.1:g.5344_5348delinsGGCATCA

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.164_168delinsGGCATCA ENSP00000494175.1:p.Val55GlyfsTer8
ENST00000335295.4:c.164_168delinsGGCATCA MANE Select ENSP00000333994.3:p.Val55GlyfsTer8
ENST00000380315.2:c.164_168delinsGGCATCA ENSP00000369671.2:p.Val55GlyfsTer8
ENST00000475226.1:n.96_100delinsGGCATCA
ENST00000485743.1:n.215_219delinsGGCATCA
ENST00000633227.1:c.148_152delinsGGCATCA ENSP00000488004.1:p.Leu50GlyfsTer6
NM_000518.4:c.164_168delinsGGCATCA NP_000509.1:p.Val55GlyfsTer8
NM_000518.5:c.164_168delinsGGCATCA MANE Select NP_000509.1:p.Val55GlyfsTer8