Canonical Allele Identifier: CA511311034
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs1600708660
MyVariant Identifiers: chr20:g.56140584A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565528A>C , CM000682.2:g.57565528A>C GRCh38
NC_000020.10:g.56140584A>C , CM000682.1:g.56140584A>C GRCh37
NC_000020.9:g.55573990A>C NCBI36
NG_008205.1:g.9448A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1593A>C MANE Select ENSP00000319814.4:p.Gly531=
ENST00000319441.5:c.1593A>C ENSP00000319814.4:p.Gly531=
ENST00000467047.1:n.4235A>C
NM_002591.3:c.1593A>C NP_002582.3:p.Gly531=
XM_011528839.1:c.1197A>C XP_011527141.1:p.Gly399=
XM_024451888.1:c.1197A>C XP_024307656.1:p.Gly399=
NM_002591.4:c.1593A>C MANE Select NP_002582.3:p.Gly531=
Search 100 bp 5'
Search 100 bp 3'