Canonical Allele Identifier: CA413720408
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77372808G>A (hg19) chrX:g.78117311G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117311G>A , CM000685.2:g.78117311G>A GRCh38
NC_000023.10:g.77372808G>A , CM000685.1:g.77372808G>A GRCh37
NC_000023.9:g.77259464G>A NCBI36
NG_008862.1:g.18143G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.418-1G>A MANE Select ENSP00000362413.4:n.418-1G>A
ENST00000644362.1:c.334-1G>A ENSP00000496140.1:n.334-1G>A
ENST00000373316.4:c.418-1G>A ENSP00000362413.4:n.418-1G>A
ENST00000491291.1:n.410-1G>A
NM_000291.3:c.418-1G>A NP_000282.1:n.418-1G>A
NM_000291.4:c.418-1G>A MANE Select NP_000282.1:n.418-1G>A
Search 100 bp 5'
Search 100 bp 3'