Canonical Allele Identifier: CA414410218
Gene: GLUD2 HGNC NCBI

Linked Data

dbSNP Id: rs1925409953
MyVariant Identifiers: chrX:g.120182260C>A (hg19) chrX:g.121048406C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.121048406C>A , CM000685.2:g.121048406C>A GRCh38
NC_000023.10:g.120182260C>A , CM000685.1:g.120182260C>A GRCh37
NC_000023.9:g.120009941C>A NCBI36
NG_016456.1:g.5799C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000328078.3:c.722C>A MANE Select ENSP00000327589.1:p.Ala241Asp
ENST00000328078.2:c.722C>A ENSP00000327589.1:p.Ala241Asp
NM_012084.3:c.722C>A NP_036216.2:p.Ala241Asp
NM_012084.4:c.722C>A MANE Select NP_036216.2:p.Ala241Asp
Search 100 bp 5'
Search 100 bp 3'