Canonical Allele Identifier: CA70816441

Gene: PLCL2

Linked Data

• dbSNP Id: rs186878518
• gnomAD v2: 3-16955287-C-A
• gnomAD v3: 3-16913795-C-A
• gnomAD v4: 3-16913795-C-A
• MyVariant Identifiers: chr3:g.16955287C>A (hg19) ; chr3:g.16913795C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16913795C>A , CM000665.2:g.16913795C>A	GRCh38
NC_000003.11:g.16955287C>A , CM000665.1:g.16955287C>A	GRCh37
NC_000003.10:g.16930291C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615277.5:c.327+28429C>A MANE Select	ENSP00000478458.1:n.327+28429C>A
ENST00000460467.1:n.439-95879C>A
ENST00000615277.4:c.327+28429C>A	ENSP00000478458.1:n.327+28429C>A
NM_001144382.1:c.327+28429C>A	NP_001137854.1:n.327+28429C>A
XM_006713073.2:c.12+14111C>A	XP_006713136.1:n.12+14111C>A
XM_006713073.3:c.12+14111C>A	XP_006713136.1:n.12+14111C>A
XM_017006022.2:c.327+28429C>A	XP_016861511.1:n.327+28429C>A
XM_017006023.1:c.327+28429C>A	XP_016861512.1:n.327+28429C>A
XM_017006024.2:c.327+28429C>A	XP_016861513.1:n.327+28429C>A
XM_017006025.1:c.-156+14111C>A	XP_016861514.1:n.-156+14111C>A
NM_001144382.2:c.327+28429C>A MANE Select	NP_001137854.1:n.327+28429C>A