Canonical Allele Identifier: CA276415363
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281860618

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173512T>A , CM000678.2:g.173512T>A GRCh38
NC_000016.9:g.223511T>A , CM000678.1:g.223511T>A GRCh37
NC_000016.8:g.163511T>A NCBI36
NG_000006.1:g.34375T>A
NG_059186.1:g.1862T>A
NG_059271.1:g.5666T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.341T>A MANE Select ENSP00000251595.6:p.Leu114His
ENST00000251595.10:c.341T>A ENSP00000251595.6:p.Leu114His
ENST00000397806.1:c.245T>A ENSP00000380908.1:p.Leu82His
ENST00000482565.1:n.477T>A
NM_000517.4:c.341T>A NP_000508.1:p.Leu114His
NM_000517.6:c.341T>A MANE Select NP_000508.1:p.Leu114His