Canonical Allele Identifier: CA2200880833

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173403G= , CM000678.2:g.173403G=	GRCh38
NC_000016.9:g.223402G= , CM000678.1:g.223402G=	GRCh37
NC_000016.8:g.163402G=	NCBI36
NG_000006.1:g.34266G=
NG_059186.1:g.1753G=
NG_059271.1:g.5557G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.301-69G= MANE Select	ENSP00000251595.6:n.301-69G=
ENST00000251595.10:c.301-69G=	ENSP00000251595.6:n.301-69G=
ENST00000397806.1:c.205-69G=	ENSP00000380908.1:n.205-69G=
ENST00000482565.1:n.437-69G=
ENST00000484216.1:n.343G=
NM_000517.4:c.301-69G=	NP_000508.1:n.301-69G=
NM_000517.6:c.301-69G= MANE Select	NP_000508.1:n.301-69G=