Canonical Allele Identifier: CA492994437

Gene: HBA1

Linked Data

• MyVariant Identifiers: chr16:g.227350C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177351C>T , CM000678.2:g.177351C>T	GRCh38
NC_000016.9:g.227350C>T , CM000678.1:g.227350C>T	GRCh37
NC_000016.8:g.167350C>T	NCBI36
NG_000006.1:g.38214C>T
NG_059186.1:g.5701C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320868.9:c.369C>T MANE Select	ENSP00000322421.5:p.His123=
ENST00000397797.1:c.273C>T	ENSP00000380899.1:p.His91=
ENST00000472694.1:n.505C>T
NM_000558.4:c.369C>T	NP_000549.1:p.His123=
NM_000558.5:c.369C>T MANE Select	NP_000549.1:p.His123=