Canonical Allele Identifier: CA339253766

Gene: PLA2G2A

Linked Data

• MyVariant Identifiers: chr1:g.20304919G>C (hg19) ; chr1:g.19978426G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978426G>C , CM000663.2:g.19978426G>C	GRCh38
NC_000001.10:g.20304919G>C , CM000663.1:g.20304919G>C	GRCh37
NC_000001.9:g.20177506G>C	NCBI36
NG_012928.1:g.7014C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000482011.3:c.139C>G MANE Select	ENSP00000504762.1:p.His47Asp
ENST00000400520.8:c.139C>G	ENSP00000383364.3:p.His47Asp
ENST00000482011.2:c.139C>G	ENSP00000504762.1:p.His47Asp
ENST00000649436.1:c.58C>G	ENSP00000496912.1:p.His20Asp
ENST00000375111.7:c.139C>G	ENSP00000364252.3:p.His47Asp
ENST00000400520.7:c.139C>G	ENSP00000383364.3:p.His47Asp
ENST00000461140.1:n.393C>G
ENST00000469162.5:n.305C>G
ENST00000482011.1:n.411C>G
ENST00000491964.5:n.371C>G
ENST00000496748.1:n.489C>G
NM_000300.3:c.139C>G	NP_000291.1:p.His47Asp
NM_001161727.1:c.139C>G	NP_001155199.1:p.His47Asp
NM_001161728.1:c.139C>G	NP_001155200.1:p.His47Asp
NM_001161729.1:c.139C>G	NP_001155201.1:p.His47Asp
NM_000300.4:c.139C>G	NP_000291.1:p.His47Asp
NM_001161727.2:c.139C>G	NP_001155199.1:p.His47Asp
NM_001161728.2:c.139C>G	NP_001155200.1:p.His47Asp
NM_001395463.1:c.139C>G MANE Select	NP_001382392.1:p.His47Asp