Canonical Allele Identifier: CA2694156216
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78123463-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123463T>A , CM000685.2:g.78123463T>A GRCh38
NC_000023.10:g.77378960T>A , CM000685.1:g.77378960T>A GRCh37
NC_000023.9:g.77265616T>A NCBI36
NG_008862.1:g.24295T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.936+89T>A MANE Select ENSP00000362413.4:n.936+89T>A
ENST00000644362.1:c.852+89T>A ENSP00000496140.1:n.852+89T>A
ENST00000373316.4:c.936+89T>A ENSP00000362413.4:n.936+89T>A
NM_000291.3:c.936+89T>A NP_000282.1:n.936+89T>A
NM_000291.4:c.936+89T>A MANE Select NP_000282.1:n.936+89T>A
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