Canonical Allele Identifier: CA16602270
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs63750404

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173510C>G , CM000678.2:g.173510C>G GRCh38
NC_000016.9:g.223509C>G , CM000678.1:g.223509C>G GRCh37
NC_000016.8:g.163509C>G NCBI36
NG_000006.1:g.34373C>G
NG_059186.1:g.1860C>G
NG_059271.1:g.5664C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.339C>G MANE Select ENSP00000251595.6:p.His113Gln
ENST00000251595.10:c.339C>G ENSP00000251595.6:p.His113Gln
ENST00000397806.1:c.243C>G ENSP00000380908.1:p.His81Gln
ENST00000482565.1:n.475C>G
NM_000517.4:c.339C>G NP_000508.1:p.His113Gln
NM_000517.6:c.339C>G MANE Select NP_000508.1:p.His113Gln