Canonical Allele Identifier: CA217113644
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs35002698

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226619C>A , CM000673.2:g.5226619C>A GRCh38
NC_000011.9:g.5247849C>A , CM000673.1:g.5247849C>A GRCh37
NC_000011.8:g.5204425C>A NCBI36
NG_000007.3:g.70997G>T
NG_059281.1:g.5453G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.273G>T ENSP00000494175.1:p.Glu91Asp
ENST00000335295.4:c.273G>T MANE Select ENSP00000333994.3:p.Glu91Asp
ENST00000475226.1:n.205G>T
ENST00000485743.1:n.324G>T
ENST00000633227.1:c.*89G>T ENSP00000488004.1:n.*89G>T
NM_000518.4:c.273G>T NP_000509.1:p.Glu91Asp
NM_000518.5:c.273G>T MANE Select NP_000509.1:p.Glu91Asp