Canonical Allele Identifier: CA409437158
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs1207210140
gnomAD v4: 20-57565370-C-A
MyVariant Identifiers: chr20:g.56140426C>A (hg19) chr20:g.57565370C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565370C>A , CM000682.2:g.57565370C>A GRCh38
NC_000020.10:g.56140426C>A , CM000682.1:g.56140426C>A GRCh37
NC_000020.9:g.55573832C>A NCBI36
NG_008205.1:g.9290C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1435C>A MANE Select ENSP00000319814.4:p.Pro479Thr
ENST00000319441.5:c.1435C>A ENSP00000319814.4:p.Pro479Thr
ENST00000467047.1:n.4077C>A
ENST00000485958.1:n.559C>A
NM_002591.3:c.1435C>A NP_002582.3:p.Pro479Thr
XM_011528839.1:c.1039C>A XP_011527141.1:p.Pro347Thr
XM_024451888.1:c.1039C>A XP_024307656.1:p.Pro347Thr
NM_002591.4:c.1435C>A MANE Select NP_002582.3:p.Pro479Thr
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