Canonical Allele Identifier: CA2711057718

Gene: EXOC2

Linked Data

• dbSNP Id: rs2127601819

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.577821G>T , CM000668.2:g.577821G>T	GRCh38
NC_000006.11:g.577821G>T , CM000668.1:g.577821G>T	GRCh37
NC_000006.10:g.522821G>T	NCBI36
NG_047166.1:g.120321C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230449.9:c.1193-939C>A MANE Select	ENSP00000230449.4:n.1193-939C>A
ENST00000230449.8:c.1193-939C>A	ENSP00000230449.4:n.1193-939C>A
NM_018303.5:c.1193-939C>A	NP_060773.3:n.1193-939C>A
NR_073064.1:n.1521-939C>A
XM_017011018.1:c.1193-939C>A	XP_016866507.1:n.1193-939C>A
XM_017011019.1:c.1193-939C>A	XP_016866508.1:n.1193-939C>A
XM_017011020.1:c.1193-939C>A	XP_016866509.1:n.1193-939C>A
XM_017011021.1:c.1193-939C>A	XP_016866510.1:n.1193-939C>A
XM_017011022.1:c.1193-939C>A	XP_016866511.1:n.1193-939C>A
XM_017011023.1:c.1193-939C>A	XP_016866512.1:n.1193-939C>A
XM_017011024.1:c.1193-939C>A	XP_016866513.1:n.1193-939C>A
XM_017011025.1:c.1193-939C>A	XP_016866514.1:n.1193-939C>A
XM_017011026.1:c.1193-939C>A	XP_016866515.1:n.1193-939C>A
NM_018303.6:c.1193-939C>A MANE Select	NP_060773.3:n.1193-939C>A
NR_073064.2:n.1519-939C>A