Canonical Allele Identifier: CA878427453
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs1482446854
gnomAD v4: X-78123102-A-T
MyVariant Identifiers: chrX:g.78123102A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123102A>T , CM000685.2:g.78123102A>T GRCh38
NC_000023.10:g.77378599A>T , CM000685.1:g.77378599A>T GRCh37
NC_000023.9:g.77265255A>T NCBI36
NG_008862.1:g.23934A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.757-93A>T MANE Select ENSP00000362413.4:n.757-93A>T
ENST00000644362.1:c.673-93A>T ENSP00000496140.1:n.673-93A>T
ENST00000373316.4:c.757-93A>T ENSP00000362413.4:n.757-93A>T
ENST00000474281.1:n.164-93A>T
NM_000291.3:c.757-93A>T NP_000282.1:n.757-93A>T
NM_000291.4:c.757-93A>T MANE Select NP_000282.1:n.757-93A>T
Search 100 bp 5'
Search 100 bp 3'