Canonical Allele Identifier: CA133331541
Gene: EXOC2 HGNC NCBI

Linked Data

dbSNP Id: rs9504361
gnomAD v2: 6-577820-A-G
gnomAD v3: 6-577820-A-G
gnomAD v4: 6-577820-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.577820A>G , CM000668.2:g.577820A>G GRCh38
NC_000006.11:g.577820A>G , CM000668.1:g.577820A>G GRCh37
NC_000006.10:g.522820A>G NCBI36
NG_047166.1:g.120322T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000230449.9:c.1193-938T>C MANE Select ENSP00000230449.4:n.1193-938T>C
ENST00000230449.8:c.1193-938T>C ENSP00000230449.4:n.1193-938T>C
NM_018303.5:c.1193-938T>C NP_060773.3:n.1193-938T>C
NR_073064.1:n.1521-938T>C
XM_017011018.1:c.1193-938T>C XP_016866507.1:n.1193-938T>C
XM_017011019.1:c.1193-938T>C XP_016866508.1:n.1193-938T>C
XM_017011020.1:c.1193-938T>C XP_016866509.1:n.1193-938T>C
XM_017011021.1:c.1193-938T>C XP_016866510.1:n.1193-938T>C
XM_017011022.1:c.1193-938T>C XP_016866511.1:n.1193-938T>C
XM_017011023.1:c.1193-938T>C XP_016866512.1:n.1193-938T>C
XM_017011024.1:c.1193-938T>C XP_016866513.1:n.1193-938T>C
XM_017011025.1:c.1193-938T>C XP_016866514.1:n.1193-938T>C
XM_017011026.1:c.1193-938T>C XP_016866515.1:n.1193-938T>C
NM_018303.6:c.1193-938T>C MANE Select NP_060773.3:n.1193-938T>C
NR_073064.2:n.1519-938T>C