Canonical Allele Identifier: CA2200882898

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.176832C= , CM000678.2:g.176832C=	GRCh38
NC_000016.9:g.226831C= , CM000678.1:g.226831C=	GRCh37
NC_000016.8:g.166831C=	NCBI36
NG_000006.1:g.37695C=
NG_059186.1:g.5182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320868.9:c.95+21C= MANE Select	ENSP00000322421.5:n.95+21C=
ENST00000397797.1:c.-2+70C=	ENSP00000380899.1:n.-2+70C=
ENST00000472694.1:n.135C=
ENST00000487791.1:n.64+21C=
NM_000558.4:c.95+21C=	NP_000549.1:n.95+21C=
NM_000558.5:c.95+21C= MANE Select	NP_000549.1:n.95+21C=