Canonical Allele Identifier: CA2847227755

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173102C>G , CM000678.2:g.173102C>G	GRCh38
NC_000016.9:g.223101C>G , CM000678.1:g.223101C>G	GRCh37
NC_000016.8:g.163101C>G	NCBI36
NG_000006.1:g.33965C>G
NG_059186.1:g.1452C>G
NG_059271.1:g.5256C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.96-23C>G MANE Select	ENSP00000251595.6:n.96-23C>G
ENST00000251595.10:c.96-23C>G	ENSP00000251595.6:n.96-23C>G
ENST00000397806.1:c.-1-23C>G	ENSP00000380908.1:n.-1-23C>G
ENST00000482565.1:n.209C>G
ENST00000484216.1:n.65-23C>G
NM_000517.4:c.96-23C>G	NP_000508.1:n.96-23C>G
NM_000517.6:c.96-23C>G MANE Select	NP_000508.1:n.96-23C>G