Canonical Allele Identifier: CA409437768
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs1600708778

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565647A>G , CM000682.2:g.57565647A>G GRCh38
NC_000020.10:g.56140703A>G , CM000682.1:g.56140703A>G GRCh37
NC_000020.9:g.55574109A>G NCBI36
NG_008205.1:g.9567A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1712A>G MANE Select ENSP00000319814.4:p.His571Arg
ENST00000319441.5:c.1712A>G ENSP00000319814.4:p.His571Arg
ENST00000467047.1:n.4354A>G
NM_002591.3:c.1712A>G NP_002582.3:p.His571Arg
XM_011528839.1:c.1316A>G XP_011527141.1:p.His439Arg
XM_024451888.1:c.1316A>G XP_024307656.1:p.His439Arg
NM_002591.4:c.1712A>G MANE Select NP_002582.3:p.His571Arg