Canonical Allele Identifier: CA2200880798

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173339G= , CM000678.2:g.173339G=	GRCh38
NC_000016.9:g.223338G= , CM000678.1:g.223338G=	GRCh37
NC_000016.8:g.163338G=	NCBI36
NG_000006.1:g.34202G=
NG_059186.1:g.1689G=
NG_059271.1:g.5493G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.300+10G= MANE Select	ENSP00000251595.6:n.300+10G=
ENST00000251595.10:c.300+10G=	ENSP00000251595.6:n.300+10G=
ENST00000397806.1:c.204+10G=	ENSP00000380908.1:n.204+10G=
ENST00000482565.1:n.436+10G=
ENST00000484216.1:n.279G=
NM_000517.4:c.300+10G=	NP_000508.1:n.300+10G=
NM_000517.6:c.300+10G= MANE Select	NP_000508.1:n.300+10G=