Canonical Allele Identifier: CA1867298243
Gene: ALG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221646G= , CM000671.2:g.99221646G= GRCh38
NC_000009.11:g.101983928G= , CM000671.1:g.101983928G= GRCh37
NC_000009.10:g.101023749G= NCBI36
NG_008928.1:g.5319C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.249C= MANE Select ENSP00000417764.1:p.Gly83=
ENST00000238477.5:c.249C= ENSP00000432675.2:p.Gly83=
ENST00000476832.1:c.249C= ENSP00000417764.1:p.Gly83=
NM_033087.3:c.249C= NP_149078.1:p.Gly83=
NR_024532.1:n.319C=
NM_033087.4:c.249C= MANE Select NP_149078.1:p.Gly83=
NR_024532.2:n.297C=
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