Canonical Allele Identifier: CA10459722
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs782350586
ExAC: X:77373501 G / T
gnomAD v2: X-77373501-G-T
gnomAD v3: X-78118004-G-T
gnomAD v4: X-78118004-G-T
MyVariant Identifiers: chrX:g.77373501G>T (hg19) chrX:g.78118004G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118004G>T , CM000685.2:g.78118004G>T GRCh38
NC_000023.10:g.77373501G>T , CM000685.1:g.77373501G>T GRCh37
NC_000023.9:g.77260157G>T NCBI36
NG_008862.1:g.18836G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.522-47G>T MANE Select ENSP00000362413.4:n.522-47G>T
ENST00000644362.1:c.438-47G>T ENSP00000496140.1:n.438-47G>T
ENST00000373316.4:c.522-47G>T ENSP00000362413.4:n.522-47G>T
ENST00000491291.1:n.514-47G>T
NM_000291.3:c.522-47G>T NP_000282.1:n.522-47G>T
NM_000291.4:c.522-47G>T MANE Select NP_000282.1:n.522-47G>T
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