Canonical Allele Identifier: CA2200882838

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.176762G= , CM000678.2:g.176762G=	GRCh38
NC_000016.9:g.226761G= , CM000678.1:g.226761G=	GRCh37
NC_000016.8:g.166761G=	NCBI36
NG_000006.1:g.37625G=
NG_059186.1:g.5112G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.46G= MANE Select	ENSP00000322421.5:p.Gly16=
ENST00000397797.1:c.-2G=	ENSP00000380899.1:n.-2G=
ENST00000472694.1:n.65G=
ENST00000487791.1:n.15G=
NM_000558.4:c.46G=	NP_000549.1:p.Gly16=
NM_000558.5:c.46G= MANE Select	NP_000549.1:p.Gly16=