Canonical Allele Identifier: CA2200883182
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177216G= , CM000678.2:g.177216G= GRCh38
NC_000016.9:g.227215G= , CM000678.1:g.227215G= GRCh37
NC_000016.8:g.167215G= NCBI36
NG_000006.1:g.38079G=
NG_059186.1:g.5566G=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.301-67G= MANE Select ENSP00000322421.5:n.301-67G=
ENST00000397797.1:c.205-67G= ENSP00000380899.1:n.205-67G=
ENST00000472694.1:n.437-67G=
ENST00000487791.1:n.352G=
NM_000558.4:c.301-67G= NP_000549.1:n.301-67G=
NM_000558.5:c.301-67G= MANE Select NP_000549.1:n.301-67G=