Canonical Allele Identifier: CA1157333470

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs2046248522

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978222T>C , CM000663.2:g.19978222T>C	GRCh38
NC_000001.10:g.20304715T>C , CM000663.1:g.20304715T>C	GRCh37
NC_000001.9:g.20177302T>C	NCBI36
NG_012928.1:g.7218A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.186-101A>G MANE Select	ENSP00000504762.1:n.186-101A>G
ENST00000400520.8:c.186-101A>G	ENSP00000383364.3:n.186-101A>G
ENST00000482011.2:c.186-101A>G	ENSP00000504762.1:n.186-101A>G
ENST00000649436.1:c.105-101A>G	ENSP00000496912.1:n.105-101A>G
ENST00000375111.7:c.186-101A>G	ENSP00000364252.3:n.186-101A>G
ENST00000400520.7:c.186-101A>G	ENSP00000383364.3:n.186-101A>G
ENST00000469162.5:n.352-101A>G
ENST00000482011.1:n.458-101A>G
ENST00000491964.5:n.418-101A>G
ENST00000496748.1:n.693A>G
NM_000300.3:c.186-101A>G	NP_000291.1:n.186-101A>G
NM_001161727.1:c.186-101A>G	NP_001155199.1:n.186-101A>G
NM_001161728.1:c.186-101A>G	NP_001155200.1:n.186-101A>G
NM_001161729.1:c.186-101A>G	NP_001155201.1:n.186-101A>G
NM_000300.4:c.186-101A>G	NP_000291.1:n.186-101A>G
NM_001161727.2:c.186-101A>G	NP_001155199.1:n.186-101A>G
NM_001161728.2:c.186-101A>G	NP_001155200.1:n.186-101A>G
NM_001395463.1:c.186-101A>G MANE Select	NP_001382392.1:n.186-101A>G