Canonical Allele Identifier: CA416639618

Gene: PLA2G2A

Linked Data

• MyVariant Identifiers: chr1:g.20304959T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978466T>G , CM000663.2:g.19978466T>G	GRCh38
NC_000001.10:g.20304959T>G , CM000663.1:g.20304959T>G	GRCh37
NC_000001.9:g.20177546T>G	NCBI36
NG_012928.1:g.6974A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.99A>C MANE Select	ENSP00000504762.1:p.Thr33=
ENST00000400520.8:c.99A>C	ENSP00000383364.3:p.Thr33=
ENST00000482011.2:c.99A>C	ENSP00000504762.1:p.Thr33=
ENST00000649436.1:c.18A>C	ENSP00000496912.1:p.Thr6=
ENST00000375111.7:c.99A>C	ENSP00000364252.3:p.Thr33=
ENST00000400520.7:c.99A>C	ENSP00000383364.3:p.Thr33=
ENST00000461140.1:n.353A>C
ENST00000469162.5:n.265A>C
ENST00000482011.1:n.371A>C
ENST00000491964.5:n.331A>C
ENST00000496748.1:n.449A>C
NM_000300.3:c.99A>C	NP_000291.1:p.Thr33=
NM_001161727.1:c.99A>C	NP_001155199.1:p.Thr33=
NM_001161728.1:c.99A>C	NP_001155200.1:p.Thr33=
NM_001161729.1:c.99A>C	NP_001155201.1:p.Thr33=
NM_000300.4:c.99A>C	NP_000291.1:p.Thr33=
NM_001161727.2:c.99A>C	NP_001155199.1:p.Thr33=
NM_001161728.2:c.99A>C	NP_001155200.1:p.Thr33=
NM_001395463.1:c.99A>C MANE Select	NP_001382392.1:p.Thr33=