Canonical Allele Identifier: CA2200882948
Gene: HBA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176890G= , CM000678.2:g.176890G= GRCh38
NC_000016.9:g.226889G= , CM000678.1:g.226889G= GRCh37
NC_000016.8:g.166889G= NCBI36
NG_000006.1:g.37753G=
NG_059186.1:g.5240G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.96-39G= MANE Select ENSP00000322421.5:n.96-39G=
ENST00000397797.1:c.-1-39G= ENSP00000380899.1:n.-1-39G=
ENST00000472694.1:n.193G=
ENST00000487791.1:n.65-39G=
NM_000558.4:c.96-39G= NP_000549.1:n.96-39G=
NM_000558.5:c.96-39G= MANE Select NP_000549.1:n.96-39G=
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