Canonical Allele Identifier: CA409437282
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs907101906
MyVariant Identifiers: chr20:g.56140482G>A (hg19) chr20:g.57565426G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565426G>A , CM000682.2:g.57565426G>A GRCh38
NC_000020.10:g.56140482G>A , CM000682.1:g.56140482G>A GRCh37
NC_000020.9:g.55573888G>A NCBI36
NG_008205.1:g.9346G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1491G>A MANE Select ENSP00000319814.4:p.Trp497Ter
ENST00000319441.5:c.1491G>A ENSP00000319814.4:p.Trp497Ter
ENST00000467047.1:n.4133G>A
NM_002591.3:c.1491G>A NP_002582.3:p.Trp497Ter
XM_011528839.1:c.1095G>A XP_011527141.1:p.Trp365Ter
XM_024451888.1:c.1095G>A XP_024307656.1:p.Trp365Ter
NM_002591.4:c.1491G>A MANE Select NP_002582.3:p.Trp497Ter
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