Canonical Allele Identifier: CA511310893
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs2146527687
MyVariant Identifiers: chr20:g.56137876C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562820C>T , CM000682.2:g.57562820C>T GRCh38
NC_000020.10:g.56137876C>T , CM000682.1:g.56137876C>T GRCh37
NC_000020.9:g.55571282C>T NCBI36
NG_008205.1:g.6740C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.531C>T MANE Select ENSP00000319814.4:p.Gly177=
ENST00000319441.5:c.531C>T ENSP00000319814.4:p.Gly177=
ENST00000467047.1:n.1741C>T
ENST00000498194.1:n.473C>T
NM_002591.3:c.531C>T NP_002582.3:p.Gly177=
XM_011528839.1:c.135C>T XP_011527141.1:p.Gly45=
XM_024451888.1:c.135C>T XP_024307656.1:p.Gly45=
NM_002591.4:c.531C>T MANE Select NP_002582.3:p.Gly177=
Search 100 bp 5'
Search 100 bp 3'