Canonical Allele Identifier: CA2630736877

Gene: HBA2

Linked Data

• gnomAD v4: 16-172902-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172902G>T , CM000678.2:g.172902G>T	GRCh38
NC_000016.9:g.222901G>T , CM000678.1:g.222901G>T	GRCh37
NC_000016.8:g.162901G>T	NCBI36
NG_000006.1:g.33765G>T
NG_059186.1:g.1252G>T
NG_059271.1:g.5056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.-11G>T MANE Select	ENSP00000251595.6:n.-11G>T
ENST00000251595.10:c.-11G>T	ENSP00000251595.6:n.-11G>T
ENST00000397806.1:c.-58G>T	ENSP00000380908.1:n.-58G>T
ENST00000482565.1:n.9G>T
NM_000517.4:c.-11G>T	NP_000508.1:n.-11G>T
NM_000517.6:c.-11G>T MANE Select	NP_000508.1:n.-11G>T