Canonical Allele Identifier: CA2200880652

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173163C= , CM000678.2:g.173163C=	GRCh38
NC_000016.9:g.223162C= , CM000678.1:g.223162C=	GRCh37
NC_000016.8:g.163162C=	NCBI36
NG_000006.1:g.34026C=
NG_059186.1:g.1513C=
NG_059271.1:g.5317C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.134C= MANE Select	ENSP00000251595.6:p.Pro45=
ENST00000251595.10:c.134C=	ENSP00000251595.6:p.Pro45=
ENST00000397806.1:c.38C=	ENSP00000380908.1:p.Pro13=
ENST00000482565.1:n.270C=
ENST00000484216.1:n.103C=
NM_000517.4:c.134C=	NP_000508.1:p.Pro45=
NM_000517.6:c.134C= MANE Select	NP_000508.1:p.Pro45=