Canonical Allele Identifier: CA379273633
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225598T>A , CM000673.2:g.5225598T>A GRCh38
NC_000011.9:g.5246828T>A , CM000673.1:g.5246828T>A GRCh37
NC_000011.8:g.5203404T>A NCBI36
NG_000007.3:g.72018A>T
NG_059281.1:g.6474A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.444A>T ENSP00000494175.1:p.Ter148Tyr
ENST00000335295.4:c.444A>T MANE Select ENSP00000333994.3:p.Ter148Tyr
ENST00000633227.1:c.*260A>T ENSP00000488004.1:n.*260A>T
NM_000518.4:c.444A>T NP_000509.1:p.Ter148Tyr
NM_000518.5:c.444A>T MANE Select NP_000509.1:p.Ter148Tyr