Canonical Allele Identifier: CA878422988
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs1218592749
gnomAD v3: X-78117215-G-C
gnomAD v4: X-78117215-G-C
MyVariant Identifiers: chrX:g.78117215G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117215G>C , CM000685.2:g.78117215G>C GRCh38
NC_000023.10:g.77372712G>C , CM000685.1:g.77372712G>C GRCh37
NC_000023.9:g.77259368G>C NCBI36
NG_008862.1:g.18047G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.418-97G>C MANE Select ENSP00000362413.4:n.418-97G>C
ENST00000644362.1:c.334-97G>C ENSP00000496140.1:n.334-97G>C
ENST00000373316.4:c.418-97G>C ENSP00000362413.4:n.418-97G>C
ENST00000491291.1:n.410-97G>C
NM_000291.3:c.418-97G>C NP_000282.1:n.418-97G>C
NM_000291.4:c.418-97G>C MANE Select NP_000282.1:n.418-97G>C
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