Canonical Allele Identifier: CA2200880909
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173501G= , CM000678.2:g.173501G= GRCh38
NC_000016.9:g.223500G= , CM000678.1:g.223500G= GRCh37
NC_000016.8:g.163500G= NCBI36
NG_000006.1:g.34364G=
NG_059186.1:g.1851G=
NG_059271.1:g.5655G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.330G= MANE Select ENSP00000251595.6:p.Leu110=
ENST00000251595.10:c.330G= ENSP00000251595.6:p.Leu110=
ENST00000397806.1:c.234G= ENSP00000380908.1:p.Leu78=
ENST00000482565.1:n.466G=
NM_000517.4:c.330G= NP_000508.1:p.Leu110=
NM_000517.6:c.330G= MANE Select NP_000508.1:p.Leu110=