Canonical Allele Identifier: CA413716641
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378775T>G (hg19) chrX:g.78123278T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123278T>G , CM000685.2:g.78123278T>G GRCh38
NC_000023.10:g.77378775T>G , CM000685.1:g.77378775T>G GRCh37
NC_000023.9:g.77265431T>G NCBI36
NG_008862.1:g.24110T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.840T>G MANE Select ENSP00000362413.4:p.Ile280Met
ENST00000644362.1:c.756T>G ENSP00000496140.1:p.Ile252Met
ENST00000373316.4:c.840T>G ENSP00000362413.4:p.Ile280Met
ENST00000474281.1:n.247T>G
NM_000291.3:c.840T>G NP_000282.1:p.Ile280Met
NM_000291.4:c.840T>G MANE Select NP_000282.1:p.Ile280Met
Search 100 bp 5'
Search 100 bp 3'