Canonical Allele Identifier: CA2200880616

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173109C= , CM000678.2:g.173109C=	GRCh38
NC_000016.9:g.223108C= , CM000678.1:g.223108C=	GRCh37
NC_000016.8:g.163108C=	NCBI36
NG_000006.1:g.33972C=
NG_059186.1:g.1459C=
NG_059271.1:g.5263C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.96-16C= MANE Select	ENSP00000251595.6:n.96-16C=
ENST00000251595.10:c.96-16C=	ENSP00000251595.6:n.96-16C=
ENST00000397806.1:c.-1-16C=	ENSP00000380908.1:n.-1-16C=
ENST00000482565.1:n.216C=
ENST00000484216.1:n.65-16C=
NM_000517.4:c.96-16C=	NP_000508.1:n.96-16C=
NM_000517.6:c.96-16C= MANE Select	NP_000508.1:n.96-16C=