Canonical Allele Identifier: CA2200880727

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173259T= , CM000678.2:g.173259T=	GRCh38
NC_000016.9:g.223258T= , CM000678.1:g.223258T=	GRCh37
NC_000016.8:g.163258T=	NCBI36
NG_000006.1:g.34122T=
NG_059186.1:g.1609T=
NG_059271.1:g.5413T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.230T= MANE Select	ENSP00000251595.6:p.Met77=
ENST00000251595.10:c.230T=	ENSP00000251595.6:p.Met77=
ENST00000397806.1:c.134T=	ENSP00000380908.1:p.Met45=
ENST00000482565.1:n.366T=
ENST00000484216.1:n.199T=
NM_000517.4:c.230T=	NP_000508.1:p.Met77=
NM_000517.6:c.230T= MANE Select	NP_000508.1:p.Met77=