Canonical Allele Identifier: CA276414515
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs951751710
gnomAD v3: 16-173113-T-G
gnomAD v4: 16-173113-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173113T>G , CM000678.2:g.173113T>G GRCh38
NC_000016.9:g.223112T>G , CM000678.1:g.223112T>G GRCh37
NC_000016.8:g.163112T>G NCBI36
NG_000006.1:g.33976T>G
NG_059186.1:g.1463T>G
NG_059271.1:g.5267T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.96-12T>G MANE Select ENSP00000251595.6:n.96-12T>G
ENST00000251595.10:c.96-12T>G ENSP00000251595.6:n.96-12T>G
ENST00000397806.1:c.-1-12T>G ENSP00000380908.1:n.-1-12T>G
ENST00000482565.1:n.220T>G
ENST00000484216.1:n.65-12T>G
NM_000517.4:c.96-12T>G NP_000508.1:n.96-12T>G
NM_000517.6:c.96-12T>G MANE Select NP_000508.1:n.96-12T>G