Canonical Allele Identifier: CA10459724
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs782123483
gnomAD v4: X-78118019-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118019A>T , CM000685.2:g.78118019A>T GRCh38
NC_000023.10:g.77373516A>T , CM000685.1:g.77373516A>T GRCh37
NC_000023.9:g.77260172A>T NCBI36
NG_008862.1:g.18851A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.522-32A>T MANE Select ENSP00000362413.4:n.522-32A>T
ENST00000644362.1:c.438-32A>T ENSP00000496140.1:n.438-32A>T
ENST00000373316.4:c.522-32A>T ENSP00000362413.4:n.522-32A>T
ENST00000491291.1:n.514-32A>T
NM_000291.3:c.522-32A>T NP_000282.1:n.522-32A>T
NM_000291.4:c.522-32A>T MANE Select NP_000282.1:n.522-32A>T