Canonical Allele Identifier: CA7506885

Gene: PLA2G4D

Linked Data

• ClinVar Variation Id: 3214138
• ClinVar RCV Id: RCV004511510
• dbSNP Id: rs765770804
• ExAC: 15:42378522 G / C
• gnomAD v2: 15-42378522-G-C
• gnomAD v3: 15-42086324-G-C
• gnomAD v4: 15-42086324-G-C
• MyVariant Identifiers: chr15:g.42378522G>C (hg19) ; chr15:g.42086324G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42086324G>C , CM000677.2:g.42086324G>C	GRCh38
NC_000015.9:g.42378522G>C , CM000677.1:g.42378522G>C	GRCh37
NC_000015.8:g.40165814G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290472.4:c.276C>G MANE Select	ENSP00000290472.3:p.Ile92Met
ENST00000290472.3:c.276C>G	ENSP00000290472.3:p.Ile92Met
NM_178034.3:c.276C>G	NP_828848.3:p.Ile92Met
XM_011521467.1:c.108C>G	XP_011519769.1:p.Ile36Met
XR_931798.1:n.376C>G
XM_011521467.2:c.108C>G	XP_011519769.1:p.Ile36Met
XR_931798.2:n.376C>G
NM_178034.4:c.276C>G MANE Select	NP_828848.3:p.Ile92Met