Canonical Allele Identifier: CA2371896185
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs2070157769

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562659T>C , CM000682.2:g.57562659T>C GRCh38
NC_000020.10:g.56137715T>C , CM000682.1:g.56137715T>C GRCh37
NC_000020.9:g.55571121T>C NCBI36
NG_008205.1:g.6579T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.407-37T>C MANE Select ENSP00000319814.4:n.407-37T>C
ENST00000319441.5:c.407-37T>C ENSP00000319814.4:n.407-37T>C
ENST00000467047.1:n.1580T>C
ENST00000498194.1:n.312T>C
NM_002591.3:c.407-37T>C NP_002582.3:n.407-37T>C
XM_011528839.1:c.11-37T>C XP_011527141.1:n.11-37T>C
XM_024451888.1:c.11-37T>C XP_024307656.1:n.11-37T>C
NM_002591.4:c.407-37T>C MANE Select NP_002582.3:n.407-37T>C