Canonical Allele Identifier: CA1867298314
Gene: ALG2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99221666G= , CM000671.2:g.99221666G= GRCh38
NC_000009.11:g.101983948G= , CM000671.1:g.101983948G= GRCh37
NC_000009.10:g.101023769G= NCBI36
NG_008928.1:g.5299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476832.2:c.229C= MANE Select ENSP00000417764.1:p.Arg77=
ENST00000238477.5:c.229C= ENSP00000432675.2:p.Arg77=
ENST00000476832.1:c.229C= ENSP00000417764.1:p.Arg77=
NM_033087.3:c.229C= NP_149078.1:p.Arg77=
NR_024532.1:n.299C=
NM_033087.4:c.229C= MANE Select NP_149078.1:p.Arg77=
NR_024532.2:n.277C=
Search 100 bp 5'
Search 100 bp 3'