Canonical Allele Identifier: CA2200880852
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173427C= , CM000678.2:g.173427C= GRCh38
NC_000016.9:g.223426C= , CM000678.1:g.223426C= GRCh37
NC_000016.8:g.163426C= NCBI36
NG_000006.1:g.34290C=
NG_059186.1:g.1777C=
NG_059271.1:g.5581C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-45C= MANE Select ENSP00000251595.6:n.301-45C=
ENST00000251595.10:c.301-45C= ENSP00000251595.6:n.301-45C=
ENST00000397806.1:c.205-45C= ENSP00000380908.1:n.205-45C=
ENST00000482565.1:n.437-45C=
ENST00000484216.1:n.367C=
NM_000517.4:c.301-45C= NP_000508.1:n.301-45C=
NM_000517.6:c.301-45C= MANE Select NP_000508.1:n.301-45C=