Canonical Allele Identifier: CA413721373
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77373558G>C (hg19) chrX:g.78118061G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118061G>C , CM000685.2:g.78118061G>C GRCh38
NC_000023.10:g.77373558G>C , CM000685.1:g.77373558G>C GRCh37
NC_000023.9:g.77260214G>C NCBI36
NG_008862.1:g.18893G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.532G>C MANE Select ENSP00000362413.4:p.Gly178Arg
ENST00000644362.1:c.448G>C ENSP00000496140.1:p.Gly150Arg
ENST00000373316.4:c.532G>C ENSP00000362413.4:p.Gly178Arg
ENST00000491291.1:n.524G>C
NM_000291.3:c.532G>C NP_000282.1:p.Gly178Arg
NM_000291.4:c.532G>C MANE Select NP_000282.1:p.Gly178Arg
Search 100 bp 5'
Search 100 bp 3'