Canonical Allele Identifier: CA339253969

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs1326977837
• gnomAD v2: 1-20305008-T-C
• gnomAD v4: 1-19978515-T-C
• MyVariant Identifiers: chr1:g.20305008T>C (hg19) ; chr1:g.19978515T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978515T>C , CM000663.2:g.19978515T>C	GRCh38
NC_000001.10:g.20305008T>C , CM000663.1:g.20305008T>C	GRCh37
NC_000001.9:g.20177595T>C	NCBI36
NG_012928.1:g.6925A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.50A>G MANE Select	ENSP00000504762.1:p.Gln17Arg
ENST00000400520.8:c.50A>G	ENSP00000383364.3:p.Gln17Arg
ENST00000482011.2:c.50A>G	ENSP00000504762.1:p.Gln17Arg
ENST00000649436.1:c.-1-31A>G	ENSP00000496912.1:n.-1-31A>G
ENST00000375111.7:c.50A>G	ENSP00000364252.3:p.Gln17Arg
ENST00000400520.7:c.50A>G	ENSP00000383364.3:p.Gln17Arg
ENST00000461140.1:n.335-31A>G
ENST00000469162.5:n.216A>G
ENST00000482011.1:n.322A>G
ENST00000491964.5:n.282A>G
ENST00000496748.1:n.400A>G
NM_000300.3:c.50A>G	NP_000291.1:p.Gln17Arg
NM_001161727.1:c.50A>G	NP_001155199.1:p.Gln17Arg
NM_001161728.1:c.50A>G	NP_001155200.1:p.Gln17Arg
NM_001161729.1:c.50A>G	NP_001155201.1:p.Gln17Arg
NM_000300.4:c.50A>G	NP_000291.1:p.Gln17Arg
NM_001161727.2:c.50A>G	NP_001155199.1:p.Gln17Arg
NM_001161728.2:c.50A>G	NP_001155200.1:p.Gln17Arg
NM_001395463.1:c.50A>G MANE Select	NP_001382392.1:p.Gln17Arg