Canonical Allele Identifier: CA729959921

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs1321216492
• gnomAD v3: 1-19978566-G-A
• gnomAD v4: 1-19978566-G-A
• MyVariant Identifiers: chr1:g.20305059G>A (hg19) ; chr1:g.19978566G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978566G>A , CM000663.2:g.19978566G>A	GRCh38
NC_000001.10:g.20305059G>A , CM000663.1:g.20305059G>A	GRCh37
NC_000001.9:g.20177646G>A	NCBI36
NG_012928.1:g.6874C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.41-42C>T MANE Select	ENSP00000504762.1:n.41-42C>T
ENST00000400520.8:c.41-42C>T	ENSP00000383364.3:n.41-42C>T
ENST00000482011.2:c.41-42C>T	ENSP00000504762.1:n.41-42C>T
ENST00000649436.1:c.-1-82C>T	ENSP00000496912.1:n.-1-82C>T
ENST00000375111.7:c.41-42C>T	ENSP00000364252.3:n.41-42C>T
ENST00000400520.7:c.41-42C>T	ENSP00000383364.3:n.41-42C>T
ENST00000461140.1:n.335-82C>T
ENST00000469162.5:n.207-42C>T
ENST00000482011.1:n.313-42C>T
ENST00000491964.5:n.273-42C>T
ENST00000496748.1:n.349C>T
NM_000300.3:c.41-42C>T	NP_000291.1:n.41-42C>T
NM_001161727.1:c.41-42C>T	NP_001155199.1:n.41-42C>T
NM_001161728.1:c.41-42C>T	NP_001155200.1:n.41-42C>T
NM_001161729.1:c.41-42C>T	NP_001155201.1:n.41-42C>T
NM_000300.4:c.41-42C>T	NP_000291.1:n.41-42C>T
NM_001161727.2:c.41-42C>T	NP_001155199.1:n.41-42C>T
NM_001161728.2:c.41-42C>T	NP_001155200.1:n.41-42C>T
NM_001395463.1:c.41-42C>T MANE Select	NP_001382392.1:n.41-42C>T