Canonical Allele Identifier: CA2694155752
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78117297-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117297T>G , CM000685.2:g.78117297T>G GRCh38
NC_000023.10:g.77372794T>G , CM000685.1:g.77372794T>G GRCh37
NC_000023.9:g.77259450T>G NCBI36
NG_008862.1:g.18129T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.418-15T>G MANE Select ENSP00000362413.4:n.418-15T>G
ENST00000644362.1:c.334-15T>G ENSP00000496140.1:n.334-15T>G
ENST00000373316.4:c.418-15T>G ENSP00000362413.4:n.418-15T>G
ENST00000491291.1:n.410-15T>G
NM_000291.3:c.418-15T>G NP_000282.1:n.418-15T>G
NM_000291.4:c.418-15T>G MANE Select NP_000282.1:n.418-15T>G