Canonical Allele Identifier: CA2200883338

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177430A= , CM000678.2:g.177430A=	GRCh38
NC_000016.9:g.227429A= , CM000678.1:g.227429A=	GRCh37
NC_000016.8:g.167429A=	NCBI36
NG_000006.1:g.38293A=
NG_059186.1:g.5780A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.*19A= MANE Select	ENSP00000322421.5:n.*19A=
ENST00000397797.1:c.*19A=	ENSP00000380899.1:n.*19A=
ENST00000472694.1:n.584A=
NM_000558.4:c.*19A=	NP_000549.1:n.*19A=
NM_000558.5:c.*19A= MANE Select	NP_000549.1:n.*19A=