Canonical Allele Identifier: CA2694156119
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78123098-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123098C>G , CM000685.2:g.78123098C>G GRCh38
NC_000023.10:g.77378595C>G , CM000685.1:g.77378595C>G GRCh37
NC_000023.9:g.77265251C>G NCBI36
NG_008862.1:g.23930C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.757-97C>G MANE Select ENSP00000362413.4:n.757-97C>G
ENST00000644362.1:c.673-97C>G ENSP00000496140.1:n.673-97C>G
ENST00000373316.4:c.757-97C>G ENSP00000362413.4:n.757-97C>G
ENST00000474281.1:n.164-97C>G
NM_000291.3:c.757-97C>G NP_000282.1:n.757-97C>G
NM_000291.4:c.757-97C>G MANE Select NP_000282.1:n.757-97C>G