Canonical Allele Identifier: CA511310858
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs1600706783
MyVariant Identifiers: chr20:g.56137816C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562760C>A , CM000682.2:g.57562760C>A GRCh38
NC_000020.10:g.56137816C>A , CM000682.1:g.56137816C>A GRCh37
NC_000020.9:g.55571222C>A NCBI36
NG_008205.1:g.6680C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.471C>A MANE Select ENSP00000319814.4:p.Gly157=
ENST00000319441.5:c.471C>A ENSP00000319814.4:p.Gly157=
ENST00000467047.1:n.1681C>A
ENST00000498194.1:n.413C>A
NM_002591.3:c.471C>A NP_002582.3:p.Gly157=
XM_011528839.1:c.75C>A XP_011527141.1:p.Gly25=
XM_024451888.1:c.75C>A XP_024307656.1:p.Gly25=
NM_002591.4:c.471C>A MANE Select NP_002582.3:p.Gly157=
Search 100 bp 5'
Search 100 bp 3'