Canonical Allele Identifier: CA413721361
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77373553T>C (hg19) chrX:g.78118056T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118056T>C , CM000685.2:g.78118056T>C GRCh38
NC_000023.10:g.77373553T>C , CM000685.1:g.77373553T>C GRCh37
NC_000023.9:g.77260209T>C NCBI36
NG_008862.1:g.18888T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.527T>C MANE Select ENSP00000362413.4:p.Met176Thr
ENST00000644362.1:c.443T>C ENSP00000496140.1:p.Met148Thr
ENST00000373316.4:c.527T>C ENSP00000362413.4:p.Met176Thr
ENST00000491291.1:n.519T>C
NM_000291.3:c.527T>C NP_000282.1:p.Met176Thr
NM_000291.4:c.527T>C MANE Select NP_000282.1:p.Met176Thr
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