Canonical Allele Identifier: CA393993642
Gene: HBA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173254C>A , CM000678.2:g.173254C>A GRCh38
NC_000016.9:g.223253C>A , CM000678.1:g.223253C>A GRCh37
NC_000016.8:g.163253C>A NCBI36
NG_000006.1:g.34117C>A
NG_059186.1:g.1604C>A
NG_059271.1:g.5408C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.225C>A MANE Select ENSP00000251595.6:p.Asp75Glu
ENST00000251595.10:c.225C>A ENSP00000251595.6:p.Asp75Glu
ENST00000397806.1:c.129C>A ENSP00000380908.1:p.Asp43Glu
ENST00000482565.1:n.361C>A
ENST00000484216.1:n.194C>A
NM_000517.4:c.225C>A NP_000508.1:p.Asp75Glu
NM_000517.6:c.225C>A MANE Select NP_000508.1:p.Asp75Glu