Canonical Allele Identifier: CA2200880841
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173412G= , CM000678.2:g.173412G= GRCh38
NC_000016.9:g.223411G= , CM000678.1:g.223411G= GRCh37
NC_000016.8:g.163411G= NCBI36
NG_000006.1:g.34275G=
NG_059186.1:g.1762G=
NG_059271.1:g.5566G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-60G= MANE Select ENSP00000251595.6:n.301-60G=
ENST00000251595.10:c.301-60G= ENSP00000251595.6:n.301-60G=
ENST00000397806.1:c.205-60G= ENSP00000380908.1:n.205-60G=
ENST00000482565.1:n.437-60G=
ENST00000484216.1:n.352G=
NM_000517.4:c.301-60G= NP_000508.1:n.301-60G=
NM_000517.6:c.301-60G= MANE Select NP_000508.1:n.301-60G=