Canonical Allele Identifier: CA2200880982

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173594C= , CM000678.2:g.173594C=	GRCh38
NC_000016.9:g.223593C= , CM000678.1:g.223593C=	GRCh37
NC_000016.8:g.163593C=	NCBI36
NG_000006.1:g.34457C=
NG_059186.1:g.1944C=
NG_059271.1:g.5748C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.423C= MANE Select	ENSP00000251595.6:p.Tyr141=
ENST00000251595.10:c.423C=	ENSP00000251595.6:p.Tyr141=
ENST00000397806.1:c.327C=	ENSP00000380908.1:p.Tyr109=
ENST00000482565.1:n.559C=
NM_000517.4:c.423C=	NP_000508.1:p.Tyr141=
NM_000517.6:c.423C= MANE Select	NP_000508.1:p.Tyr141=