Canonical Allele Identifier: CA2694156160
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78123171-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123171C>T , CM000685.2:g.78123171C>T GRCh38
NC_000023.10:g.77378668C>T , CM000685.1:g.77378668C>T GRCh37
NC_000023.9:g.77265324C>T NCBI36
NG_008862.1:g.24003C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.757-24C>T MANE Select ENSP00000362413.4:n.757-24C>T
ENST00000644362.1:c.673-24C>T ENSP00000496140.1:n.673-24C>T
ENST00000373316.4:c.757-24C>T ENSP00000362413.4:n.757-24C>T
ENST00000474281.1:n.164-24C>T
NM_000291.3:c.757-24C>T NP_000282.1:n.757-24C>T
NM_000291.4:c.757-24C>T MANE Select NP_000282.1:n.757-24C>T