Canonical Allele Identifier: CA125247
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15396
ClinVar RCV Id: RCV000016649
dbSNP Id: rs33958637

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225717T>C , CM000673.2:g.5225717T>C GRCh38
NC_000011.9:g.5246947T>C , CM000673.1:g.5246947T>C GRCh37
NC_000011.8:g.5203523T>C NCBI36
NG_000007.3:g.71899A>G
NG_059281.1:g.6355A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.325A>G ENSP00000494175.1:p.Asn109Asp
ENST00000335295.4:c.325A>G MANE Select ENSP00000333994.3:p.Asn109Asp
ENST00000475226.1:n.257A>G
ENST00000633227.1:c.*141A>G ENSP00000488004.1:n.*141A>G
NM_000518.4:c.325A>G NP_000509.1:p.Asn109Asp
NM_000518.5:c.325A>G MANE Select NP_000509.1:p.Asn109Asp