Canonical Allele Identifier: CA2200880634

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173140C= , CM000678.2:g.173140C=	GRCh38
NC_000016.9:g.223139C= , CM000678.1:g.223139C=	GRCh37
NC_000016.8:g.163139C=	NCBI36
NG_000006.1:g.34003C=
NG_059186.1:g.1490C=
NG_059271.1:g.5294C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.111C= MANE Select	ENSP00000251595.6:p.Phe37=
ENST00000251595.10:c.111C=	ENSP00000251595.6:p.Phe37=
ENST00000397806.1:c.15C=	ENSP00000380908.1:p.Phe5=
ENST00000482565.1:n.247C=
ENST00000484216.1:n.80C=
NM_000517.4:c.111C=	NP_000508.1:p.Phe37=
NM_000517.6:c.111C= MANE Select	NP_000508.1:p.Phe37=