Canonical Allele Identifier: CA2694155969
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78118296-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118296T>G , CM000685.2:g.78118296T>G GRCh38
NC_000023.10:g.77373793T>G , CM000685.1:g.77373793T>G GRCh37
NC_000023.9:g.77260449T>G NCBI36
NG_008862.1:g.19128T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.641+126T>G MANE Select ENSP00000362413.4:n.641+126T>G
ENST00000644362.1:c.557+126T>G ENSP00000496140.1:n.557+126T>G
ENST00000373316.4:c.641+126T>G ENSP00000362413.4:n.641+126T>G
ENST00000491291.1:n.633+126T>G
NM_000291.3:c.641+126T>G NP_000282.1:n.641+126T>G
NM_000291.4:c.641+126T>G MANE Select NP_000282.1:n.641+126T>G
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