Canonical Allele Identifier: CA413721173
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs868923506
gnomAD v3: X-78117370-A-G
gnomAD v4: X-78117370-A-G
MyVariant Identifiers: chrX:g.77372867A>G (hg19) chrX:g.78117370A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117370A>G , CM000685.2:g.78117370A>G GRCh38
NC_000023.10:g.77372867A>G , CM000685.1:g.77372867A>G GRCh37
NC_000023.9:g.77259523A>G NCBI36
NG_008862.1:g.18202A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.476A>G MANE Select ENSP00000362413.4:p.Asp159Gly
ENST00000644362.1:c.392A>G ENSP00000496140.1:p.Asp131Gly
ENST00000373316.4:c.476A>G ENSP00000362413.4:p.Asp159Gly
ENST00000491291.1:n.468A>G
NM_000291.3:c.476A>G NP_000282.1:p.Asp159Gly
NM_000291.4:c.476A>G MANE Select NP_000282.1:p.Asp159Gly
Search 100 bp 5'
Search 100 bp 3'