Canonical Allele Identifier: CA878427844
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs1251462107
gnomAD v3: X-78123474-C-T
gnomAD v4: X-78123474-C-T
MyVariant Identifiers: chrX:g.78123474C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123474C>T , CM000685.2:g.78123474C>T GRCh38
NC_000023.10:g.77378971C>T , CM000685.1:g.77378971C>T GRCh37
NC_000023.9:g.77265627C>T NCBI36
NG_008862.1:g.24306C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.936+100C>T MANE Select ENSP00000362413.4:n.936+100C>T
ENST00000644362.1:c.852+100C>T ENSP00000496140.1:n.852+100C>T
ENST00000373316.4:c.936+100C>T ENSP00000362413.4:n.936+100C>T
NM_000291.3:c.936+100C>T NP_000282.1:n.936+100C>T
NM_000291.4:c.936+100C>T MANE Select NP_000282.1:n.936+100C>T
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