Canonical Allele Identifier: CA517380813
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378787T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123290T>C , CM000685.2:g.78123290T>C GRCh38
NC_000023.10:g.77378787T>C , CM000685.1:g.77378787T>C GRCh37
NC_000023.9:g.77265443T>C NCBI36
NG_008862.1:g.24122T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.852T>C MANE Select ENSP00000362413.4:p.Val284=
ENST00000644362.1:c.768T>C ENSP00000496140.1:p.Val256=
ENST00000373316.4:c.852T>C ENSP00000362413.4:p.Val284=
ENST00000474281.1:n.259T>C
NM_000291.3:c.852T>C NP_000282.1:p.Val284=
NM_000291.4:c.852T>C MANE Select NP_000282.1:p.Val284=
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