Canonical Allele Identifier: CA2439140464
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs2078364678
gnomAD v4: X-78123131-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123131T>C , CM000685.2:g.78123131T>C GRCh38
NC_000023.10:g.77378628T>C , CM000685.1:g.77378628T>C GRCh37
NC_000023.9:g.77265284T>C NCBI36
NG_008862.1:g.23963T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.757-64T>C MANE Select ENSP00000362413.4:n.757-64T>C
ENST00000644362.1:c.673-64T>C ENSP00000496140.1:n.673-64T>C
ENST00000373316.4:c.757-64T>C ENSP00000362413.4:n.757-64T>C
ENST00000474281.1:n.164-64T>C
NM_000291.3:c.757-64T>C NP_000282.1:n.757-64T>C
NM_000291.4:c.757-64T>C MANE Select NP_000282.1:n.757-64T>C