Canonical Allele Identifier: CA2200881058

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173698T= , CM000678.2:g.173698T=	GRCh38
NC_000016.9:g.223697T= , CM000678.1:g.223697T=	GRCh37
NC_000016.8:g.163697T=	NCBI36
NG_000006.1:g.34561T=
NG_059186.1:g.2048T=
NG_059271.1:g.5852T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.*98T= MANE Select	ENSP00000251595.6:n.*98T=
ENST00000251595.10:c.*98T=	ENSP00000251595.6:n.*98T=
ENST00000397806.1:c.*98T=	ENSP00000380908.1:n.*98T=
NM_000517.4:c.*98T=	NP_000508.1:n.*98T=
NM_000517.6:c.*98T= MANE Select	NP_000508.1:n.*98T=