Canonical Allele Identifier: CA658065

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs776668415
• ExAC: 1:20305031 T / C
• gnomAD v2: 1-20305031-T-C
• gnomAD v4: 1-19978538-T-C
• MyVariant Identifiers: chr1:g.20305031T>C (hg19) ; chr1:g.19978538T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978538T>C , CM000663.2:g.19978538T>C	GRCh38
NC_000001.10:g.20305031T>C , CM000663.1:g.20305031T>C	GRCh37
NC_000001.9:g.20177618T>C	NCBI36
NG_012928.1:g.6902A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.41-14A>G MANE Select	ENSP00000504762.1:n.41-14A>G
ENST00000400520.8:c.41-14A>G	ENSP00000383364.3:n.41-14A>G
ENST00000482011.2:c.41-14A>G	ENSP00000504762.1:n.41-14A>G
ENST00000649436.1:c.-1-54A>G	ENSP00000496912.1:n.-1-54A>G
ENST00000375111.7:c.41-14A>G	ENSP00000364252.3:n.41-14A>G
ENST00000400520.7:c.41-14A>G	ENSP00000383364.3:n.41-14A>G
ENST00000461140.1:n.335-54A>G
ENST00000469162.5:n.207-14A>G
ENST00000482011.1:n.313-14A>G
ENST00000491964.5:n.273-14A>G
ENST00000496748.1:n.377A>G
NM_000300.3:c.41-14A>G	NP_000291.1:n.41-14A>G
NM_001161727.1:c.41-14A>G	NP_001155199.1:n.41-14A>G
NM_001161728.1:c.41-14A>G	NP_001155200.1:n.41-14A>G
NM_001161729.1:c.41-14A>G	NP_001155201.1:n.41-14A>G
NM_000300.4:c.41-14A>G	NP_000291.1:n.41-14A>G
NM_001161727.2:c.41-14A>G	NP_001155199.1:n.41-14A>G
NM_001161728.2:c.41-14A>G	NP_001155200.1:n.41-14A>G
NM_001395463.1:c.41-14A>G MANE Select	NP_001382392.1:n.41-14A>G