Canonical Allele Identifier: CA339253796

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs1207872960
• MyVariant Identifiers: chr1:g.20304933C>A (hg19) ; chr1:g.19978440C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978440C>A , CM000663.2:g.19978440C>A	GRCh38
NC_000001.10:g.20304933C>A , CM000663.1:g.20304933C>A	GRCh37
NC_000001.9:g.20177520C>A	NCBI36
NG_012928.1:g.7000G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000482011.3:c.125G>T MANE Select	ENSP00000504762.1:p.Gly42Val
ENST00000400520.8:c.125G>T	ENSP00000383364.3:p.Gly42Val
ENST00000482011.2:c.125G>T	ENSP00000504762.1:p.Gly42Val
ENST00000649436.1:c.44G>T	ENSP00000496912.1:p.Gly15Val
ENST00000375111.7:c.125G>T	ENSP00000364252.3:p.Gly42Val
ENST00000400520.7:c.125G>T	ENSP00000383364.3:p.Gly42Val
ENST00000461140.1:n.379G>T
ENST00000469162.5:n.291G>T
ENST00000482011.1:n.397G>T
ENST00000491964.5:n.357G>T
ENST00000496748.1:n.475G>T
NM_000300.3:c.125G>T	NP_000291.1:p.Gly42Val
NM_001161727.1:c.125G>T	NP_001155199.1:p.Gly42Val
NM_001161728.1:c.125G>T	NP_001155200.1:p.Gly42Val
NM_001161729.1:c.125G>T	NP_001155201.1:p.Gly42Val
NM_000300.4:c.125G>T	NP_000291.1:p.Gly42Val
NM_001161727.2:c.125G>T	NP_001155199.1:p.Gly42Val
NM_001161728.2:c.125G>T	NP_001155200.1:p.Gly42Val
NM_001395463.1:c.125G>T MANE Select	NP_001382392.1:p.Gly42Val