Canonical Allele Identifier: CA379273697
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225665G>T , CM000673.2:g.5225665G>T GRCh38
NC_000011.9:g.5246895G>T , CM000673.1:g.5246895G>T GRCh37
NC_000011.8:g.5203471G>T NCBI36
NG_000007.3:g.71951C>A
NG_059281.1:g.6407C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.377C>A ENSP00000494175.1:p.Pro126Gln
ENST00000335295.4:c.377C>A MANE Select ENSP00000333994.3:p.Pro126Gln
ENST00000475226.1:n.309C>A
ENST00000633227.1:c.*193C>A ENSP00000488004.1:n.*193C>A
NM_000518.4:c.377C>A NP_000509.1:p.Pro126Gln
NM_000518.5:c.377C>A MANE Select NP_000509.1:p.Pro126Gln