Canonical Allele Identifier: CA393993822

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.223291A>T (hg19) ; chr16:g.173292A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173292A>T , CM000678.2:g.173292A>T	GRCh38
NC_000016.9:g.223291A>T , CM000678.1:g.223291A>T	GRCh37
NC_000016.8:g.163291A>T	NCBI36
NG_000006.1:g.34155A>T
NG_059186.1:g.1642A>T
NG_059271.1:g.5446A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.263A>T MANE Select	ENSP00000251595.6:p.His88Leu
ENST00000251595.10:c.263A>T	ENSP00000251595.6:p.His88Leu
ENST00000397806.1:c.167A>T	ENSP00000380908.1:p.His56Leu
ENST00000482565.1:n.399A>T
ENST00000484216.1:n.232A>T
NM_000517.4:c.263A>T	NP_000508.1:p.His88Leu
NM_000517.6:c.263A>T MANE Select	NP_000508.1:p.His88Leu