Canonical Allele Identifier: CA2630736871

Gene: HBA2

Linked Data

• gnomAD v4: 16-172895-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172895A>T , CM000678.2:g.172895A>T	GRCh38
NC_000016.9:g.222894A>T , CM000678.1:g.222894A>T	GRCh37
NC_000016.8:g.162894A>T	NCBI36
NG_000006.1:g.33758A>T
NG_059186.1:g.1245A>T
NG_059271.1:g.5049A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.-18A>T MANE Select	ENSP00000251595.6:n.-18A>T
ENST00000251595.10:c.-18A>T	ENSP00000251595.6:n.-18A>T
ENST00000397806.1:c.-65A>T	ENSP00000380908.1:n.-65A>T
ENST00000482565.1:n.2A>T
NM_000517.4:c.-18A>T	NP_000508.1:n.-18A>T
NM_000517.6:c.-18A>T MANE Select	NP_000508.1:n.-18A>T