Canonical Allele Identifier: CA19255218

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs767563899
• gnomAD v3: 1-19978571-G-C
• gnomAD v4: 1-19978571-G-C
• MyVariant Identifiers: chr1:g.20305064G>C (hg19) ; chr1:g.19978571G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978571G>C , CM000663.2:g.19978571G>C	GRCh38
NC_000001.10:g.20305064G>C , CM000663.1:g.20305064G>C	GRCh37
NC_000001.9:g.20177651G>C	NCBI36
NG_012928.1:g.6869C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.41-47C>G MANE Select	ENSP00000504762.1:n.41-47C>G
ENST00000400520.8:c.41-47C>G	ENSP00000383364.3:n.41-47C>G
ENST00000482011.2:c.41-47C>G	ENSP00000504762.1:n.41-47C>G
ENST00000649436.1:c.-1-87C>G	ENSP00000496912.1:n.-1-87C>G
ENST00000375111.7:c.41-47C>G	ENSP00000364252.3:n.41-47C>G
ENST00000400520.7:c.41-47C>G	ENSP00000383364.3:n.41-47C>G
ENST00000461140.1:n.335-87C>G
ENST00000469162.5:n.207-47C>G
ENST00000482011.1:n.313-47C>G
ENST00000491964.5:n.273-47C>G
ENST00000496748.1:n.344C>G
NM_000300.3:c.41-47C>G	NP_000291.1:n.41-47C>G
NM_001161727.1:c.41-47C>G	NP_001155199.1:n.41-47C>G
NM_001161728.1:c.41-47C>G	NP_001155200.1:n.41-47C>G
NM_001161729.1:c.41-47C>G	NP_001155201.1:n.41-47C>G
NM_000300.4:c.41-47C>G	NP_000291.1:n.41-47C>G
NM_001161727.2:c.41-47C>G	NP_001155199.1:n.41-47C>G
NM_001161728.2:c.41-47C>G	NP_001155200.1:n.41-47C>G
NM_001395463.1:c.41-47C>G MANE Select	NP_001382392.1:n.41-47C>G