Canonical Allele Identifier: CA2200880907
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173499C= , CM000678.2:g.173499C= GRCh38
NC_000016.9:g.223498C= , CM000678.1:g.223498C= GRCh37
NC_000016.8:g.163498C= NCBI36
NG_000006.1:g.34362C=
NG_059186.1:g.1849C=
NG_059271.1:g.5653C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.328C= MANE Select ENSP00000251595.6:p.Leu110=
ENST00000251595.10:c.328C= ENSP00000251595.6:p.Leu110=
ENST00000397806.1:c.232C= ENSP00000380908.1:p.Leu78=
ENST00000482565.1:n.464C=
NM_000517.4:c.328C= NP_000508.1:p.Leu110=
NM_000517.6:c.328C= MANE Select NP_000508.1:p.Leu110=