Canonical Allele Identifier: CA2200883188
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177225C= , CM000678.2:g.177225C= GRCh38
NC_000016.9:g.227224C= , CM000678.1:g.227224C= GRCh37
NC_000016.8:g.167224C= NCBI36
NG_000006.1:g.38088C=
NG_059186.1:g.5575C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.301-58C= MANE Select ENSP00000322421.5:n.301-58C=
ENST00000397797.1:c.205-58C= ENSP00000380899.1:n.205-58C=
ENST00000472694.1:n.437-58C=
ENST00000487791.1:n.361C=
NM_000558.4:c.301-58C= NP_000549.1:n.301-58C=
NM_000558.5:c.301-58C= MANE Select NP_000549.1:n.301-58C=