Canonical Allele Identifier: CA2200883018

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.176987G= , CM000678.2:g.176987G=	GRCh38
NC_000016.9:g.226986G= , CM000678.1:g.226986G=	GRCh37
NC_000016.8:g.166986G=	NCBI36
NG_000006.1:g.37850G=
NG_059186.1:g.5337G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.154G= MANE Select	ENSP00000322421.5:p.Gly52=
ENST00000397797.1:c.58G=	ENSP00000380899.1:p.Gly20=
ENST00000472694.1:n.290G=
ENST00000487791.1:n.123G=
NM_000558.4:c.154G=	NP_000549.1:p.Gly52=
NM_000558.5:c.154G= MANE Select	NP_000549.1:p.Gly52=