Canonical Allele Identifier: CA217112360
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs33984863

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225633C>A , CM000673.2:g.5225633C>A GRCh38
NC_000011.9:g.5246863C>A , CM000673.1:g.5246863C>A GRCh37
NC_000011.8:g.5203439C>A NCBI36
NG_000007.3:g.71983G>T
NG_059281.1:g.6439G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.409G>T ENSP00000494175.1:p.Gly137Cys
ENST00000335295.4:c.409G>T MANE Select ENSP00000333994.3:p.Gly137Cys
ENST00000633227.1:c.*225G>T ENSP00000488004.1:n.*225G>T
NM_000518.4:c.409G>T NP_000509.1:p.Gly137Cys
NM_000518.5:c.409G>T MANE Select NP_000509.1:p.Gly137Cys