Canonical Allele Identifier: CA2200881051

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173680T= , CM000678.2:g.173680T=	GRCh38
NC_000016.9:g.223679T= , CM000678.1:g.223679T=	GRCh37
NC_000016.8:g.163679T=	NCBI36
NG_000006.1:g.34543T=
NG_059186.1:g.2030T=
NG_059271.1:g.5834T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.*80T= MANE Select	ENSP00000251595.6:n.*80T=
ENST00000251595.10:c.*80T=	ENSP00000251595.6:n.*80T=
ENST00000397806.1:c.*80T=	ENSP00000380908.1:n.*80T=
NM_000517.4:c.*80T=	NP_000508.1:n.*80T=
NM_000517.6:c.*80T= MANE Select	NP_000508.1:n.*80T=