Canonical Allele Identifier: CA2200880586
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1902040941

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173072A>G , CM000678.2:g.173072A>G GRCh38
NC_000016.9:g.223071A>G , CM000678.1:g.223071A>G GRCh37
NC_000016.8:g.163071A>G NCBI36
NG_000006.1:g.33935A>G
NG_059186.1:g.1422A>G
NG_059271.1:g.5226A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-53A>G MANE Select ENSP00000251595.6:n.96-53A>G
ENST00000251595.10:c.96-53A>G ENSP00000251595.6:n.96-53A>G
ENST00000397806.1:c.-1-53A>G ENSP00000380908.1:n.-1-53A>G
ENST00000482565.1:n.179A>G
ENST00000484216.1:n.65-53A>G
NM_000517.4:c.96-53A>G NP_000508.1:n.96-53A>G
NM_000517.6:c.96-53A>G MANE Select NP_000508.1:n.96-53A>G