Canonical Allele Identifier: CA409434982
Gene: PCK1 HGNC NCBI

Linked Data

gnomAD v3: 20-57562715-C-G
gnomAD v4: 20-57562715-C-G
MyVariant Identifiers: chr20:g.56137771C>G (hg19) chr20:g.57562715C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562715C>G , CM000682.2:g.57562715C>G GRCh38
NC_000020.10:g.56137771C>G , CM000682.1:g.56137771C>G GRCh37
NC_000020.9:g.55571177C>G NCBI36
NG_008205.1:g.6635C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.426C>G MANE Select ENSP00000319814.4:p.Ile142Met
ENST00000319441.5:c.426C>G ENSP00000319814.4:p.Ile142Met
ENST00000467047.1:n.1636C>G
ENST00000498194.1:n.368C>G
NM_002591.3:c.426C>G NP_002582.3:p.Ile142Met
XM_011528839.1:c.30C>G XP_011527141.1:p.Ile10Met
XM_024451888.1:c.30C>G XP_024307656.1:p.Ile10Met
NM_002591.4:c.426C>G MANE Select NP_002582.3:p.Ile142Met
Search 100 bp 5'
Search 100 bp 3'