Canonical Allele Identifier: CA374231604
Gene: ALG2 HGNC NCBI

Linked Data

gnomAD v4: 9-99221638-G-T
MyVariant Identifiers: chr9:g.101983920G>T (hg19) chr9:g.99221638G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221638G>T , CM000671.2:g.99221638G>T GRCh38
NC_000009.11:g.101983920G>T , CM000671.1:g.101983920G>T GRCh37
NC_000009.10:g.101023741G>T NCBI36
NG_008928.1:g.5327C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.257C>A MANE Select ENSP00000417764.1:p.Ala86Asp
ENST00000238477.5:c.257C>A ENSP00000432675.2:p.Ala86Asp
ENST00000476832.1:c.257C>A ENSP00000417764.1:p.Ala86Asp
NM_033087.3:c.257C>A NP_149078.1:p.Ala86Asp
NR_024532.1:n.327C>A
NM_033087.4:c.257C>A MANE Select NP_149078.1:p.Ala86Asp
NR_024532.2:n.305C>A
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