Canonical Allele Identifier: CA2200882981
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176937T= , CM000678.2:g.176937T= GRCh38
NC_000016.9:g.226936T= , CM000678.1:g.226936T= GRCh37
NC_000016.8:g.166936T= NCBI36
NG_000006.1:g.37800T=
NG_059186.1:g.5287T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.104T= MANE Select ENSP00000322421.5:p.Leu35=
ENST00000397797.1:c.8T= ENSP00000380899.1:p.Leu3=
ENST00000472694.1:n.240T=
ENST00000487791.1:n.73T=
NM_000558.4:c.104T= NP_000549.1:p.Leu35=
NM_000558.5:c.104T= MANE Select NP_000549.1:p.Leu35=