Canonical Allele Identifier: CA19255953

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs745531262
• gnomAD v2: 1-20306059-C-T
• gnomAD v3: 1-19979566-C-T
• gnomAD v4: 1-19979566-C-T
• MyVariant Identifiers: chr1:g.20306059C>T (hg19) ; chr1:g.19979566C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19979566C>T , CM000663.2:g.19979566C>T	GRCh38
NC_000001.10:g.20306059C>T , CM000663.1:g.20306059C>T	GRCh37
NC_000001.9:g.20178646C>T	NCBI36
NG_012928.1:g.5874G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.-107+14G>A MANE Select	ENSP00000504762.1:n.-107+14G>A
ENST00000400520.8:c.-139+14G>A	ENSP00000383364.3:n.-139+14G>A
ENST00000482011.2:c.-107+14G>A	ENSP00000504762.1:n.-107+14G>A
ENST00000649436.1:c.-148+14G>A	ENSP00000496912.1:n.-148+14G>A
ENST00000375111.7:c.-107+14G>A	ENSP00000364252.3:n.-107+14G>A
ENST00000400520.7:c.-107+14G>A	ENSP00000383364.3:n.-107+14G>A
ENST00000469162.5:n.28+14G>A
ENST00000482011.1:n.166+14G>A
ENST00000491964.5:n.126+14G>A
ENST00000496748.1:n.35+14G>A
NM_000300.3:c.-107+14G>A	NP_000291.1:n.-107+14G>A
NM_001161727.1:c.-107+14G>A	NP_001155199.1:n.-107+14G>A
NM_001161728.1:c.-106-687G>A	NP_001155200.1:n.-106-687G>A
NM_001161729.1:c.-139+14G>A	NP_001155201.1:n.-139+14G>A
NM_000300.4:c.-107+14G>A	NP_000291.1:n.-107+14G>A
NM_001161727.2:c.-107+14G>A	NP_001155199.1:n.-107+14G>A
NM_001161728.2:c.-106-687G>A	NP_001155200.1:n.-106-687G>A
NM_001395463.1:c.-107+14G>A MANE Select	NP_001382392.1:n.-107+14G>A