Canonical Allele Identifier: CA466648929
Gene: ALG2 HGNC NCBI

Linked Data

gnomAD v4: 9-99221580-G-T
MyVariant Identifiers: chr9:g.101983862G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221580G>T , CM000671.2:g.99221580G>T GRCh38
NC_000009.11:g.101983862G>T , CM000671.1:g.101983862G>T GRCh37
NC_000009.10:g.101023683G>T NCBI36
NG_008928.1:g.5385C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.315C>A MANE Select ENSP00000417764.1:p.Ala105=
ENST00000238477.5:c.315C>A ENSP00000432675.2:p.Ala105=
ENST00000476832.1:c.315C>A ENSP00000417764.1:p.Ala105=
NM_033087.3:c.315C>A NP_149078.1:p.Ala105=
NR_024532.1:n.385C>A
NM_033087.4:c.315C>A MANE Select NP_149078.1:p.Ala105=
NR_024532.2:n.363C>A
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