Canonical Allele Identifier: CA2200880789

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173331T= , CM000678.2:g.173331T=	GRCh38
NC_000016.9:g.223330T= , CM000678.1:g.223330T=	GRCh37
NC_000016.8:g.163330T=	NCBI36
NG_000006.1:g.34194T=
NG_059186.1:g.1681T=
NG_059271.1:g.5485T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.300+2T= MANE Select	ENSP00000251595.6:n.300+2T=
ENST00000251595.10:c.300+2T=	ENSP00000251595.6:n.300+2T=
ENST00000397806.1:c.204+2T=	ENSP00000380908.1:n.204+2T=
ENST00000482565.1:n.436+2T=
ENST00000484216.1:n.271T=
NM_000517.4:c.300+2T=	NP_000508.1:n.300+2T=
NM_000517.6:c.300+2T= MANE Select	NP_000508.1:n.300+2T=