Canonical Allele Identifier: CA2200880791

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173333A= , CM000678.2:g.173333A=	GRCh38
NC_000016.9:g.223332A= , CM000678.1:g.223332A=	GRCh37
NC_000016.8:g.163332A=	NCBI36
NG_000006.1:g.34196A=
NG_059186.1:g.1683A=
NG_059271.1:g.5487A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.300+4A= MANE Select	ENSP00000251595.6:n.300+4A=
ENST00000251595.10:c.300+4A=	ENSP00000251595.6:n.300+4A=
ENST00000397806.1:c.204+4A=	ENSP00000380908.1:n.204+4A=
ENST00000482565.1:n.436+4A=
ENST00000484216.1:n.273A=
NM_000517.4:c.300+4A=	NP_000508.1:n.300+4A=
NM_000517.6:c.300+4A= MANE Select	NP_000508.1:n.300+4A=