Canonical Allele Identifier: CA413718962
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369308A>T (hg19) chrX:g.78113811A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113811A>T , CM000685.2:g.78113811A>T GRCh38
NC_000023.10:g.77369308A>T , CM000685.1:g.77369308A>T GRCh37
NC_000023.9:g.77255964A>T NCBI36
NG_008862.1:g.14643A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.184A>T MANE Select ENSP00000362413.4:p.Ser62Cys
ENST00000644362.1:c.100A>T ENSP00000496140.1:p.Ser34Cys
ENST00000373316.4:c.184A>T ENSP00000362413.4:p.Ser62Cys
ENST00000477335.5:n.320A>T
ENST00000491291.1:n.176A>T
NM_000291.3:c.184A>T NP_000282.1:p.Ser62Cys
NM_000291.4:c.184A>T MANE Select NP_000282.1:p.Ser62Cys
Search 100 bp 5'
Search 100 bp 3'