Canonical Allele Identifier: CA492785058

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.223476A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173477A>T , CM000678.2:g.173477A>T	GRCh38
NC_000016.9:g.223476A>T , CM000678.1:g.223476A>T	GRCh37
NC_000016.8:g.163476A>T	NCBI36
NG_000006.1:g.34340A>T
NG_059186.1:g.1827A>T
NG_059271.1:g.5631A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.306A>T MANE Select	ENSP00000251595.6:p.Leu102=
ENST00000251595.10:c.306A>T	ENSP00000251595.6:p.Leu102=
ENST00000397806.1:c.210A>T	ENSP00000380908.1:p.Leu70=
ENST00000482565.1:n.442A>T
NM_000517.4:c.306A>T	NP_000508.1:p.Leu102=
NM_000517.6:c.306A>T MANE Select	NP_000508.1:p.Leu102=