Canonical Allele Identifier: CA393994470
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173511-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173511C>T , CM000678.2:g.173511C>T GRCh38
NC_000016.9:g.223510C>T , CM000678.1:g.223510C>T GRCh37
NC_000016.8:g.163510C>T NCBI36
NG_000006.1:g.34374C>T
NG_059186.1:g.1861C>T
NG_059271.1:g.5665C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.340C>T MANE Select ENSP00000251595.6:p.Leu114Phe
ENST00000251595.10:c.340C>T ENSP00000251595.6:p.Leu114Phe
ENST00000397806.1:c.244C>T ENSP00000380908.1:p.Leu82Phe
ENST00000482565.1:n.476C>T
NM_000517.4:c.340C>T NP_000508.1:p.Leu114Phe
NM_000517.6:c.340C>T MANE Select NP_000508.1:p.Leu114Phe