Canonical Allele Identifier: CA658042

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs771678574
• ExAC: 1:20304918 T / C
• gnomAD v2: 1-20304918-T-C
• gnomAD v4: 1-19978425-T-C
• MyVariant Identifiers: chr1:g.20304918T>C (hg19) ; chr1:g.19978425T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978425T>C , CM000663.2:g.19978425T>C	GRCh38
NC_000001.10:g.20304918T>C , CM000663.1:g.20304918T>C	GRCh37
NC_000001.9:g.20177505T>C	NCBI36
NG_012928.1:g.7015A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000482011.3:c.140A>G MANE Select	ENSP00000504762.1:p.His47Arg
ENST00000400520.8:c.140A>G	ENSP00000383364.3:p.His47Arg
ENST00000482011.2:c.140A>G	ENSP00000504762.1:p.His47Arg
ENST00000649436.1:c.59A>G	ENSP00000496912.1:p.His20Arg
ENST00000375111.7:c.140A>G	ENSP00000364252.3:p.His47Arg
ENST00000400520.7:c.140A>G	ENSP00000383364.3:p.His47Arg
ENST00000461140.1:n.394A>G
ENST00000469162.5:n.306A>G
ENST00000482011.1:n.412A>G
ENST00000491964.5:n.372A>G
ENST00000496748.1:n.490A>G
NM_000300.3:c.140A>G	NP_000291.1:p.His47Arg
NM_001161727.1:c.140A>G	NP_001155199.1:p.His47Arg
NM_001161728.1:c.140A>G	NP_001155200.1:p.His47Arg
NM_001161729.1:c.140A>G	NP_001155201.1:p.His47Arg
NM_000300.4:c.140A>G	NP_000291.1:p.His47Arg
NM_001161727.2:c.140A>G	NP_001155199.1:p.His47Arg
NM_001161728.2:c.140A>G	NP_001155200.1:p.His47Arg
NM_001395463.1:c.140A>G MANE Select	NP_001382392.1:p.His47Arg