Canonical Allele Identifier: CA10655706
Gene: PLCH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2477686

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2461209G>C , CM000663.2:g.2461209G>C GRCh38
NC_000001.10:g.2392648G>C , CM000663.1:g.2392648G>C GRCh37
NC_000001.9:g.2382508G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011542449.1:c.365-17267G>C XP_011540751.1:p.=
XM_011542450.1:c.365-17267G>C XP_011540752.1:p.=
XM_011542452.1:c.31+17237G>C XP_011540754.1:p.=
XM_011542454.1:c.365-17267G>C XP_011540756.1:p.=
XM_011542455.1:c.116-17267G>C XP_011540757.1:p.=
XM_011542456.1:c.116-17267G>C XP_011540758.1:p.=
XM_011542457.1:c.365-17267G>C XP_011540759.1:p.=
XM_011542459.1:c.365-17267G>C XP_011540761.1:p.=
XM_011542460.1:c.365-17267G>C XP_011540762.1:p.=
XR_946803.1:n.392-17267G>C
XM_017002870.1:c.410-17267G>C XP_016858359.1:p.=
XM_017002872.1:c.410-17267G>C XP_016858361.1:p.=
XM_017002873.1:c.410-17267G>C XP_016858362.1:p.=
XM_017002874.1:c.410-17267G>C XP_016858363.1:p.=
XM_024451058.1:c.386-17267G>C XP_024306826.1:p.=
XM_024451059.1:c.410-17267G>C XP_024306827.1:p.=
XM_024451060.1:c.116-17267G>C XP_024306828.1:p.=
XM_024451061.1:c.116-17267G>C XP_024306829.1:p.=
XM_024451062.1:c.410-17267G>C XP_024306830.1:p.=
XM_024451063.1:c.410-17267G>C XP_024306831.1:p.=
XM_024451064.1:c.410-17267G>C XP_024306832.1:p.=
ENST00000609981.5:c.116-17267G>C ENSP00000476436.1:p.=