Canonical Allele Identifier: CA393995133
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs281864501

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176984C>A , CM000678.2:g.176984C>A GRCh38
NC_000016.9:g.226983C>A , CM000678.1:g.226983C>A GRCh37
NC_000016.8:g.166983C>A NCBI36
NG_000006.1:g.37847C>A
NG_059186.1:g.5334C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.151C>A MANE Select ENSP00000322421.5:p.His51Asn
ENST00000397797.1:c.55C>A ENSP00000380899.1:p.His19Asn
ENST00000472694.1:n.287C>A
ENST00000487791.1:n.120C>A
NM_000558.4:c.151C>A NP_000549.1:p.His51Asn
NM_000558.5:c.151C>A MANE Select NP_000549.1:p.His51Asn