Canonical Allele Identifier: CA2200880679
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173197T= , CM000678.2:g.173197T= GRCh38
NC_000016.9:g.223196T= , CM000678.1:g.223196T= GRCh37
NC_000016.8:g.163196T= NCBI36
NG_000006.1:g.34060T=
NG_059186.1:g.1547T=
NG_059271.1:g.5351T=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.168T= MANE Select ENSP00000251595.6:p.Val56=
ENST00000251595.10:c.168T= ENSP00000251595.6:p.Val56=
ENST00000397806.1:c.72T= ENSP00000380908.1:p.Val24=
ENST00000482565.1:n.304T=
ENST00000484216.1:n.137T=
NM_000517.4:c.168T= NP_000508.1:p.Val56=
NM_000517.6:c.168T= MANE Select NP_000508.1:p.Val56=