Canonical Allele Identifier: CA413721630
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77373658T>G (hg19) chrX:g.78118161T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118161T>G , CM000685.2:g.78118161T>G GRCh38
NC_000023.10:g.77373658T>G , CM000685.1:g.77373658T>G GRCh37
NC_000023.9:g.77260314T>G NCBI36
NG_008862.1:g.18993T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.632T>G MANE Select ENSP00000362413.4:p.Ile211Ser
ENST00000644362.1:c.548T>G ENSP00000496140.1:p.Ile183Ser
ENST00000373316.4:c.632T>G ENSP00000362413.4:p.Ile211Ser
ENST00000491291.1:n.624T>G
NM_000291.3:c.632T>G NP_000282.1:p.Ile211Ser
NM_000291.4:c.632T>G MANE Select NP_000282.1:p.Ile211Ser
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