Canonical Allele Identifier: CA2694155965
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78118292-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118292G>T , CM000685.2:g.78118292G>T GRCh38
NC_000023.10:g.77373789G>T , CM000685.1:g.77373789G>T GRCh37
NC_000023.9:g.77260445G>T NCBI36
NG_008862.1:g.19124G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.641+122G>T MANE Select ENSP00000362413.4:n.641+122G>T
ENST00000644362.1:c.557+122G>T ENSP00000496140.1:n.557+122G>T
ENST00000373316.4:c.641+122G>T ENSP00000362413.4:n.641+122G>T
ENST00000491291.1:n.633+122G>T
NM_000291.3:c.641+122G>T NP_000282.1:n.641+122G>T
NM_000291.4:c.641+122G>T MANE Select NP_000282.1:n.641+122G>T