Canonical Allele Identifier: CA878423587
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs1242237384
gnomAD v3: X-78117952-T-A
gnomAD v4: X-78117952-T-A
MyVariant Identifiers: chrX:g.78117952T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117952T>A , CM000685.2:g.78117952T>A GRCh38
NC_000023.10:g.77373449T>A , CM000685.1:g.77373449T>A GRCh37
NC_000023.9:g.77260105T>A NCBI36
NG_008862.1:g.18784T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.522-99T>A MANE Select ENSP00000362413.4:n.522-99T>A
ENST00000644362.1:c.438-99T>A ENSP00000496140.1:n.438-99T>A
ENST00000373316.4:c.522-99T>A ENSP00000362413.4:n.522-99T>A
ENST00000491291.1:n.514-99T>A
NM_000291.3:c.522-99T>A NP_000282.1:n.522-99T>A
NM_000291.4:c.522-99T>A MANE Select NP_000282.1:n.522-99T>A
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