Canonical Allele Identifier: CA1134520966
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs2078331264
gnomAD v3: X-78117304-C-T
gnomAD v4: X-78117304-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117304C>T , CM000685.2:g.78117304C>T GRCh38
NC_000023.10:g.77372801C>T , CM000685.1:g.77372801C>T GRCh37
NC_000023.9:g.77259457C>T NCBI36
NG_008862.1:g.18136C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.418-8C>T MANE Select ENSP00000362413.4:n.418-8C>T
ENST00000644362.1:c.334-8C>T ENSP00000496140.1:n.334-8C>T
ENST00000373316.4:c.418-8C>T ENSP00000362413.4:n.418-8C>T
ENST00000491291.1:n.410-8C>T
NM_000291.3:c.418-8C>T NP_000282.1:n.418-8C>T
NM_000291.4:c.418-8C>T MANE Select NP_000282.1:n.418-8C>T