Canonical Allele Identifier: CA393993341
Gene: HBA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173161C>A , CM000678.2:g.173161C>A GRCh38
NC_000016.9:g.223160C>A , CM000678.1:g.223160C>A GRCh37
NC_000016.8:g.163160C>A NCBI36
NG_000006.1:g.34024C>A
NG_059186.1:g.1511C>A
NG_059271.1:g.5315C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.132C>A MANE Select ENSP00000251595.6:p.Phe44Leu
ENST00000251595.10:c.132C>A ENSP00000251595.6:p.Phe44Leu
ENST00000397806.1:c.36C>A ENSP00000380908.1:p.Phe12Leu
ENST00000482565.1:n.268C>A
ENST00000484216.1:n.101C>A
NM_000517.4:c.132C>A NP_000508.1:p.Phe44Leu
NM_000517.6:c.132C>A MANE Select NP_000508.1:p.Phe44Leu