Canonical Allele Identifier: CA2200880826

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173393A= , CM000678.2:g.173393A=	GRCh38
NC_000016.9:g.223392A= , CM000678.1:g.223392A=	GRCh37
NC_000016.8:g.163392A=	NCBI36
NG_000006.1:g.34256A=
NG_059186.1:g.1743A=
NG_059271.1:g.5547A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.300+64A= MANE Select	ENSP00000251595.6:n.300+64A=
ENST00000251595.10:c.300+64A=	ENSP00000251595.6:n.300+64A=
ENST00000397806.1:c.204+64A=	ENSP00000380908.1:n.204+64A=
ENST00000482565.1:n.436+64A=
ENST00000484216.1:n.333A=
NM_000517.4:c.300+64A=	NP_000508.1:n.300+64A=
NM_000517.6:c.300+64A= MANE Select	NP_000508.1:n.300+64A=