Canonical Allele Identifier: CA2200883021
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176995C= , CM000678.2:g.176995C= GRCh38
NC_000016.9:g.226994C= , CM000678.1:g.226994C= GRCh37
NC_000016.8:g.166994C= NCBI36
NG_000006.1:g.37858C=
NG_059186.1:g.5345C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.162C= MANE Select ENSP00000322421.5:p.Ala54=
ENST00000397797.1:c.66C= ENSP00000380899.1:p.Ala22=
ENST00000472694.1:n.298C=
ENST00000487791.1:n.131C=
NM_000558.4:c.162C= NP_000549.1:p.Ala54=
NM_000558.5:c.162C= MANE Select NP_000549.1:p.Ala54=