Canonical Allele Identifier: CA379274415
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226733A>C , CM000673.2:g.5226733A>C GRCh38
NC_000011.9:g.5247963A>C , CM000673.1:g.5247963A>C GRCh37
NC_000011.8:g.5204539A>C NCBI36
NG_000007.3:g.70883T>G
NG_059281.1:g.5339T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.159T>G ENSP00000494175.1:p.Asp53Glu
ENST00000335295.4:c.159T>G MANE Select ENSP00000333994.3:p.Asp53Glu
ENST00000380315.2:c.159T>G ENSP00000369671.2:p.Asp53Glu
ENST00000475226.1:n.91T>G
ENST00000485743.1:n.210T>G
ENST00000633227.1:c.143T>G ENSP00000488004.1:p.Met48Arg
NM_000518.4:c.159T>G NP_000509.1:p.Asp53Glu
NM_000518.5:c.159T>G MANE Select NP_000509.1:p.Asp53Glu