Canonical Allele Identifier: CA466648991
Gene: ALG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101983901C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221619C>T , CM000671.2:g.99221619C>T GRCh38
NC_000009.11:g.101983901C>T , CM000671.1:g.101983901C>T GRCh37
NC_000009.10:g.101023722C>T NCBI36
NG_008928.1:g.5346G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.276G>A MANE Select ENSP00000417764.1:p.Val92=
ENST00000238477.5:c.276G>A ENSP00000432675.2:p.Val92=
ENST00000476832.1:c.276G>A ENSP00000417764.1:p.Val92=
NM_033087.3:c.276G>A NP_149078.1:p.Val92=
NR_024532.1:n.346G>A
NM_033087.4:c.276G>A MANE Select NP_149078.1:p.Val92=
NR_024532.2:n.324G>A
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