Canonical Allele Identifier: CA393995800
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177299T>G , CM000678.2:g.177299T>G GRCh38
NC_000016.9:g.227298T>G , CM000678.1:g.227298T>G GRCh37
NC_000016.8:g.167298T>G NCBI36
NG_000006.1:g.38162T>G
NG_059186.1:g.5649T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.317T>G MANE Select ENSP00000322421.5:p.Leu106Arg
ENST00000397797.1:c.221T>G ENSP00000380899.1:p.Leu74Arg
ENST00000472694.1:n.453T>G
NM_000558.4:c.317T>G NP_000549.1:p.Leu106Arg
NM_000558.5:c.317T>G MANE Select NP_000549.1:p.Leu106Arg