Canonical Allele Identifier: CA393993472

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.223206G>T (hg19) ; chr16:g.173207G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173207G>T , CM000678.2:g.173207G>T	GRCh38
NC_000016.9:g.223206G>T , CM000678.1:g.223206G>T	GRCh37
NC_000016.8:g.163206G>T	NCBI36
NG_000006.1:g.34070G>T
NG_059186.1:g.1557G>T
NG_059271.1:g.5361G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.178G>T MANE Select	ENSP00000251595.6:p.Gly60Cys
ENST00000251595.10:c.178G>T	ENSP00000251595.6:p.Gly60Cys
ENST00000397806.1:c.82G>T	ENSP00000380908.1:p.Gly28Cys
ENST00000482565.1:n.314G>T
ENST00000484216.1:n.147G>T
NM_000517.4:c.178G>T	NP_000508.1:p.Gly60Cys
NM_000517.6:c.178G>T MANE Select	NP_000508.1:p.Gly60Cys