Canonical Allele Identifier: CA2575852750
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173010G>A , CM000678.2:g.173010G>A GRCh38
NC_000016.9:g.223009G>A , CM000678.1:g.223009G>A GRCh37
NC_000016.8:g.163009G>A NCBI36
NG_000006.1:g.33873G>A
NG_059186.1:g.1360G>A
NG_059271.1:g.5164G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.95+3G>A MANE Select ENSP00000251595.6:n.95+3G>A
ENST00000251595.10:c.95+3G>A ENSP00000251595.6:n.95+3G>A
ENST00000397806.1:c.-2+52G>A ENSP00000380908.1:n.-2+52G>A
ENST00000482565.1:n.117G>A
ENST00000484216.1:n.64+3G>A
NM_000517.4:c.95+3G>A NP_000508.1:n.95+3G>A
NM_000517.6:c.95+3G>A MANE Select NP_000508.1:n.95+3G>A