Canonical Allele Identifier: CA902310251
Gene: PLCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1190039386
MyVariant Identifiers: chr3:g.16938575G>A (hg19) chr3:g.16897077G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.16897077G>A , CM000665.2:g.16897077G>A GRCh38
NC_000003.11:g.16938575G>A , CM000665.1:g.16938575G>A GRCh37
NC_000003.10:g.16913579G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000615277.5:c.327+11711G>A MANE Select ENSP00000478458.1:n.327+11711G>A
ENST00000460467.1:n.438+93989G>A
ENST00000615277.4:c.327+11711G>A ENSP00000478458.1:n.327+11711G>A
NM_001144382.1:c.327+11711G>A NP_001137854.1:n.327+11711G>A
XM_006713073.3:c.-2596G>A XP_006713136.1:n.-2596G>A
XM_017006022.2:c.327+11711G>A XP_016861511.1:n.327+11711G>A
XM_017006023.1:c.327+11711G>A XP_016861512.1:n.327+11711G>A
XM_017006024.2:c.327+11711G>A XP_016861513.1:n.327+11711G>A
XM_017006025.1:c.-2763G>A XP_016861514.1:n.-2763G>A
NM_001144382.2:c.327+11711G>A MANE Select NP_001137854.1:n.327+11711G>A
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