Canonical Allele Identifier: CA10459738
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs782239577
ExAC: X:77373697 A / C
gnomAD v2: X-77373697-A-C
gnomAD v3: X-78118200-A-C
gnomAD v4: X-78118200-A-C
MyVariant Identifiers: chrX:g.77373697A>C (hg19) chrX:g.78118200A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118200A>C , CM000685.2:g.78118200A>C GRCh38
NC_000023.10:g.77373697A>C , CM000685.1:g.77373697A>C GRCh37
NC_000023.9:g.77260353A>C NCBI36
NG_008862.1:g.19032A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.641+30A>C MANE Select ENSP00000362413.4:n.641+30A>C
ENST00000644362.1:c.557+30A>C ENSP00000496140.1:n.557+30A>C
ENST00000373316.4:c.641+30A>C ENSP00000362413.4:n.641+30A>C
ENST00000491291.1:n.633+30A>C
NM_000291.3:c.641+30A>C NP_000282.1:n.641+30A>C
NM_000291.4:c.641+30A>C MANE Select NP_000282.1:n.641+30A>C
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