Canonical Allele Identifier: CA19255130

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs2236770
• MyVariant Identifiers: chr1:g.20304965C>G (hg19) ; chr1:g.19978472C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978472C>G , CM000663.2:g.19978472C>G	GRCh38
NC_000001.10:g.20304965C>G , CM000663.1:g.20304965C>G	GRCh37
NC_000001.9:g.20177552C>G	NCBI36
NG_012928.1:g.6968G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.93G>C MANE Select	ENSP00000504762.1:p.Leu31Phe
ENST00000400520.8:c.93G>C	ENSP00000383364.3:p.Leu31Phe
ENST00000482011.2:c.93G>C	ENSP00000504762.1:p.Leu31Phe
ENST00000649436.1:c.12G>C	ENSP00000496912.1:p.Leu4Phe
ENST00000375111.7:c.93G>C	ENSP00000364252.3:p.Leu31Phe
ENST00000400520.7:c.93G>C	ENSP00000383364.3:p.Leu31Phe
ENST00000461140.1:n.347G>C
ENST00000469162.5:n.259G>C
ENST00000482011.1:n.365G>C
ENST00000491964.5:n.325G>C
ENST00000496748.1:n.443G>C
NM_000300.3:c.93G>C	NP_000291.1:p.Leu31Phe
NM_001161727.1:c.93G>C	NP_001155199.1:p.Leu31Phe
NM_001161728.1:c.93G>C	NP_001155200.1:p.Leu31Phe
NM_001161729.1:c.93G>C	NP_001155201.1:p.Leu31Phe
NM_000300.4:c.93G>C	NP_000291.1:p.Leu31Phe
NM_001161727.2:c.93G>C	NP_001155199.1:p.Leu31Phe
NM_001161728.2:c.93G>C	NP_001155200.1:p.Leu31Phe
NM_001395463.1:c.93G>C MANE Select	NP_001382392.1:p.Leu31Phe