Canonical Allele Identifier: CA2575852833
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173419A>G , CM000678.2:g.173419A>G GRCh38
NC_000016.9:g.223418A>G , CM000678.1:g.223418A>G GRCh37
NC_000016.8:g.163418A>G NCBI36
NG_000006.1:g.34282A>G
NG_059186.1:g.1769A>G
NG_059271.1:g.5573A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-53A>G MANE Select ENSP00000251595.6:n.301-53A>G
ENST00000251595.10:c.301-53A>G ENSP00000251595.6:n.301-53A>G
ENST00000397806.1:c.205-53A>G ENSP00000380908.1:n.205-53A>G
ENST00000482565.1:n.437-53A>G
ENST00000484216.1:n.359A>G
NM_000517.4:c.301-53A>G NP_000508.1:n.301-53A>G
NM_000517.6:c.301-53A>G MANE Select NP_000508.1:n.301-53A>G