Canonical Allele Identifier: CA19255146

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs1045400415
• gnomAD v4: 1-19978481-C-T
• MyVariant Identifiers: chr1:g.20304974C>T (hg19) ; chr1:g.19978481C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978481C>T , CM000663.2:g.19978481C>T	GRCh38
NC_000001.10:g.20304974C>T , CM000663.1:g.20304974C>T	GRCh37
NC_000001.9:g.20177561C>T	NCBI36
NG_012928.1:g.6959G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.84G>A MANE Select	ENSP00000504762.1:p.Met28Ile
ENST00000400520.8:c.84G>A	ENSP00000383364.3:p.Met28Ile
ENST00000482011.2:c.84G>A	ENSP00000504762.1:p.Met28Ile
ENST00000649436.1:c.3G>A	ENSP00000496912.1:p.Met1Ile
ENST00000375111.7:c.84G>A	ENSP00000364252.3:p.Met28Ile
ENST00000400520.7:c.84G>A	ENSP00000383364.3:p.Met28Ile
ENST00000461140.1:n.338G>A
ENST00000469162.5:n.250G>A
ENST00000482011.1:n.356G>A
ENST00000491964.5:n.316G>A
ENST00000496748.1:n.434G>A
NM_000300.3:c.84G>A	NP_000291.1:p.Met28Ile
NM_001161727.1:c.84G>A	NP_001155199.1:p.Met28Ile
NM_001161728.1:c.84G>A	NP_001155200.1:p.Met28Ile
NM_001161729.1:c.84G>A	NP_001155201.1:p.Met28Ile
NM_000300.4:c.84G>A	NP_000291.1:p.Met28Ile
NM_001161727.2:c.84G>A	NP_001155199.1:p.Met28Ile
NM_001161728.2:c.84G>A	NP_001155200.1:p.Met28Ile
NM_001395463.1:c.84G>A MANE Select	NP_001382392.1:p.Met28Ile