Canonical Allele Identifier: CA393993391
Gene: HBA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173178G>T , CM000678.2:g.173178G>T GRCh38
NC_000016.9:g.223177G>T , CM000678.1:g.223177G>T GRCh37
NC_000016.8:g.163177G>T NCBI36
NG_000006.1:g.34041G>T
NG_059186.1:g.1528G>T
NG_059271.1:g.5332G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.149G>T MANE Select ENSP00000251595.6:p.Ser50Ile
ENST00000251595.10:c.149G>T ENSP00000251595.6:p.Ser50Ile
ENST00000397806.1:c.53G>T ENSP00000380908.1:p.Ser18Ile
ENST00000482565.1:n.285G>T
ENST00000484216.1:n.118G>T
NM_000517.4:c.149G>T NP_000508.1:p.Ser50Ile
NM_000517.6:c.149G>T MANE Select NP_000508.1:p.Ser50Ile