Canonical Allele Identifier: CA70814582

Gene: PLCL2

Linked Data

• dbSNP Id: rs756107241
• gnomAD v3: 3-16897031-T-C
• gnomAD v4: 3-16897031-T-C
• MyVariant Identifiers: chr3:g.16938529T>C (hg19) ; chr3:g.16897031T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16897031T>C , CM000665.2:g.16897031T>C	GRCh38
NC_000003.11:g.16938529T>C , CM000665.1:g.16938529T>C	GRCh37
NC_000003.10:g.16913533T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615277.5:c.327+11665T>C MANE Select	ENSP00000478458.1:n.327+11665T>C
ENST00000460467.1:n.438+93943T>C
ENST00000615277.4:c.327+11665T>C	ENSP00000478458.1:n.327+11665T>C
NM_001144382.1:c.327+11665T>C	NP_001137854.1:n.327+11665T>C
XM_006713073.3:c.-2642T>C	XP_006713136.1:n.-2642T>C
XM_017006022.2:c.327+11665T>C	XP_016861511.1:n.327+11665T>C
XM_017006023.1:c.327+11665T>C	XP_016861512.1:n.327+11665T>C
XM_017006024.2:c.327+11665T>C	XP_016861513.1:n.327+11665T>C
XM_017006025.1:c.-2809T>C	XP_016861514.1:n.-2809T>C
NM_001144382.2:c.327+11665T>C MANE Select	NP_001137854.1:n.327+11665T>C