Canonical Allele Identifier: CA2200880628
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173132C= , CM000678.2:g.173132C= GRCh38
NC_000016.9:g.223131C= , CM000678.1:g.223131C= GRCh37
NC_000016.8:g.163131C= NCBI36
NG_000006.1:g.33995C=
NG_059186.1:g.1482C=
NG_059271.1:g.5286C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.103C= MANE Select ENSP00000251595.6:p.Leu35=
ENST00000251595.10:c.103C= ENSP00000251595.6:p.Leu35=
ENST00000397806.1:c.7C= ENSP00000380908.1:p.Leu3=
ENST00000482565.1:n.239C=
ENST00000484216.1:n.72C=
NM_000517.4:c.103C= NP_000508.1:p.Leu35=
NM_000517.6:c.103C= MANE Select NP_000508.1:p.Leu35=