Canonical Allele Identifier: CA2200880329
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172968G= , CM000678.2:g.172968G= GRCh38
NC_000016.9:g.222967G= , CM000678.1:g.222967G= GRCh37
NC_000016.8:g.162967G= NCBI36
NG_000006.1:g.33831G=
NG_059186.1:g.1318G=
NG_059271.1:g.5122G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.56G= MANE Select ENSP00000251595.6:p.Gly19=
ENST00000251595.10:c.56G= ENSP00000251595.6:p.Gly19=
ENST00000397806.1:c.-2+10G= ENSP00000380908.1:n.-2+10G=
ENST00000482565.1:n.75G=
ENST00000484216.1:n.25G=
NM_000517.4:c.56G= NP_000508.1:p.Gly19=
NM_000517.6:c.56G= MANE Select NP_000508.1:p.Gly19=