Canonical Allele Identifier: CA2200883336
Gene: HBA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177423G= , CM000678.2:g.177423G= GRCh38
NC_000016.9:g.227422G= , CM000678.1:g.227422G= GRCh37
NC_000016.8:g.167422G= NCBI36
NG_000006.1:g.38286G=
NG_059186.1:g.5773G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.*12G= MANE Select ENSP00000322421.5:n.*12G=
ENST00000397797.1:c.*12G= ENSP00000380899.1:n.*12G=
ENST00000472694.1:n.577G=
NM_000558.4:c.*12G= NP_000549.1:n.*12G=
NM_000558.5:c.*12G= MANE Select NP_000549.1:n.*12G=
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