Canonical Allele Identifier: CA374231555
Gene: ALG2 HGNC NCBI

Linked Data

dbSNP Id: rs1828804380
gnomAD v3: 9-99221630-A-C
gnomAD v4: 9-99221630-A-C
MyVariant Identifiers: chr9:g.101983912A>C (hg19) chr9:g.99221630A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221630A>C , CM000671.2:g.99221630A>C GRCh38
NC_000009.11:g.101983912A>C , CM000671.1:g.101983912A>C GRCh37
NC_000009.10:g.101023733A>C NCBI36
NG_008928.1:g.5335T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.265T>G MANE Select ENSP00000417764.1:p.Cys89Gly
ENST00000238477.5:c.265T>G ENSP00000432675.2:p.Cys89Gly
ENST00000476832.1:c.265T>G ENSP00000417764.1:p.Cys89Gly
NM_033087.3:c.265T>G NP_149078.1:p.Cys89Gly
NR_024532.1:n.335T>G
NM_033087.4:c.265T>G MANE Select NP_149078.1:p.Cys89Gly
NR_024532.2:n.313T>G
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