Canonical Allele Identifier: CA2580591703
Gene: EXOC2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000230449.9:c.1193-938T>A MANE Select ENSP00000230449.4:n.1193-938T>A
ENST00000230449.8:c.1193-938T>A ENSP00000230449.4:n.1193-938T>A
NM_018303.5:c.1193-938T>A NP_060773.3:n.1193-938T>A
NR_073064.1:n.1521-938T>A
XM_017011018.1:c.1193-938T>A XP_016866507.1:n.1193-938T>A
XM_017011019.1:c.1193-938T>A XP_016866508.1:n.1193-938T>A
XM_017011020.1:c.1193-938T>A XP_016866509.1:n.1193-938T>A
XM_017011021.1:c.1193-938T>A XP_016866510.1:n.1193-938T>A
XM_017011022.1:c.1193-938T>A XP_016866511.1:n.1193-938T>A
XM_017011023.1:c.1193-938T>A XP_016866512.1:n.1193-938T>A
XM_017011024.1:c.1193-938T>A XP_016866513.1:n.1193-938T>A
XM_017011025.1:c.1193-938T>A XP_016866514.1:n.1193-938T>A
XM_017011026.1:c.1193-938T>A XP_016866515.1:n.1193-938T>A
NM_018303.6:c.1193-938T>A MANE Select NP_060773.3:n.1193-938T>A
NR_073064.2:n.1519-938T>A
Search 100 bp 5'
Search 100 bp 3'