Canonical Allele Identifier: CA492994531
Gene: HBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.227012C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177013C>A , CM000678.2:g.177013C>A GRCh38
NC_000016.9:g.227012C>A , CM000678.1:g.227012C>A GRCh37
NC_000016.8:g.167012C>A NCBI36
NG_000006.1:g.37876C>A
NG_059186.1:g.5363C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.180C>A MANE Select ENSP00000322421.5:p.Gly60=
ENST00000397797.1:c.84C>A ENSP00000380899.1:p.Gly28=
ENST00000472694.1:n.316C>A
ENST00000487791.1:n.149C>A
NM_000558.4:c.180C>A NP_000549.1:p.Gly60=
NM_000558.5:c.180C>A MANE Select NP_000549.1:p.Gly60=
Search 100 bp 5'
Search 100 bp 3'