Canonical Allele Identifier: CA2694156130
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78123123-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123123C>T , CM000685.2:g.78123123C>T GRCh38
NC_000023.10:g.77378620C>T , CM000685.1:g.77378620C>T GRCh37
NC_000023.9:g.77265276C>T NCBI36
NG_008862.1:g.23955C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.757-72C>T MANE Select ENSP00000362413.4:n.757-72C>T
ENST00000644362.1:c.673-72C>T ENSP00000496140.1:n.673-72C>T
ENST00000373316.4:c.757-72C>T ENSP00000362413.4:n.757-72C>T
ENST00000474281.1:n.164-72C>T
NM_000291.3:c.757-72C>T NP_000282.1:n.757-72C>T
NM_000291.4:c.757-72C>T MANE Select NP_000282.1:n.757-72C>T