Canonical Allele Identifier: CA413719031
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369323C>G (hg19) chrX:g.78113826C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113826C>G , CM000685.2:g.78113826C>G GRCh38
NC_000023.10:g.77369323C>G , CM000685.1:g.77369323C>G GRCh37
NC_000023.9:g.77255979C>G NCBI36
NG_008862.1:g.14658C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.199C>G MANE Select ENSP00000362413.4:p.Pro67Ala
ENST00000644362.1:c.115C>G ENSP00000496140.1:p.Pro39Ala
ENST00000373316.4:c.199C>G ENSP00000362413.4:p.Pro67Ala
ENST00000477335.5:n.335C>G
ENST00000491291.1:n.191C>G
NM_000291.3:c.199C>G NP_000282.1:p.Pro67Ala
NM_000291.4:c.199C>G MANE Select NP_000282.1:p.Pro67Ala
Search 100 bp 5'
Search 100 bp 3'