Canonical Allele Identifier: CA413717006
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78123360-C-T
MyVariant Identifiers: chrX:g.77378857C>T (hg19) chrX:g.78123360C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123360C>T , CM000685.2:g.78123360C>T GRCh38
NC_000023.10:g.77378857C>T , CM000685.1:g.77378857C>T GRCh37
NC_000023.9:g.77265513C>T NCBI36
NG_008862.1:g.24192C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.922C>T MANE Select ENSP00000362413.4:p.Pro308Ser
ENST00000644362.1:c.838C>T ENSP00000496140.1:p.Pro280Ser
ENST00000373316.4:c.922C>T ENSP00000362413.4:p.Pro308Ser
NM_000291.3:c.922C>T NP_000282.1:p.Pro308Ser
NM_000291.4:c.922C>T MANE Select NP_000282.1:p.Pro308Ser
Search 100 bp 5'
Search 100 bp 3'