Canonical Allele Identifier: CA492994550

Gene: HBA1

Linked Data

• MyVariant Identifiers: chr16:g.227024C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177025C>G , CM000678.2:g.177025C>G	GRCh38
NC_000016.9:g.227024C>G , CM000678.1:g.227024C>G	GRCh37
NC_000016.8:g.167024C>G	NCBI36
NG_000006.1:g.37888C>G
NG_059186.1:g.5375C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320868.9:c.192C>G MANE Select	ENSP00000322421.5:p.Ala64=
ENST00000397797.1:c.96C>G	ENSP00000380899.1:p.Ala32=
ENST00000472694.1:n.328C>G
ENST00000487791.1:n.161C>G
NM_000558.4:c.192C>G	NP_000549.1:p.Ala64=
NM_000558.5:c.192C>G MANE Select	NP_000549.1:p.Ala64=