Canonical Allele Identifier: CA393995648
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177128T>A , CM000678.2:g.177128T>A GRCh38
NC_000016.9:g.227127T>A , CM000678.1:g.227127T>A GRCh37
NC_000016.8:g.167127T>A NCBI36
NG_000006.1:g.37991T>A
NG_059186.1:g.5478T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.295T>A MANE Select ENSP00000322421.5:p.Phe99Ile
ENST00000397797.1:c.199T>A ENSP00000380899.1:p.Phe67Ile
ENST00000472694.1:n.431T>A
ENST00000487791.1:n.264T>A
NM_000558.4:c.295T>A NP_000549.1:p.Phe99Ile
NM_000558.5:c.295T>A MANE Select NP_000549.1:p.Phe99Ile