Canonical Allele Identifier: CA2200880710

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173237G= , CM000678.2:g.173237G=	GRCh38
NC_000016.9:g.223236G= , CM000678.1:g.223236G=	GRCh37
NC_000016.8:g.163236G=	NCBI36
NG_000006.1:g.34100G=
NG_059186.1:g.1587G=
NG_059271.1:g.5391G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.208G= MANE Select	ENSP00000251595.6:p.Ala70=
ENST00000251595.10:c.208G=	ENSP00000251595.6:p.Ala70=
ENST00000397806.1:c.112G=	ENSP00000380908.1:p.Ala38=
ENST00000482565.1:n.344G=
ENST00000484216.1:n.177G=
NM_000517.4:c.208G=	NP_000508.1:p.Ala70=
NM_000517.6:c.208G= MANE Select	NP_000508.1:p.Ala70=