Canonical Allele Identifier: CA826198006

Gene: EXOC2

Linked Data

• dbSNP Id: rs1378464117
• gnomAD v3: 6-577787-T-C
• gnomAD v4: 6-577787-T-C
• MyVariant Identifiers: chr6:g.577787T>C (hg19) ; chr6:g.577787T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.577787T>C , CM000668.2:g.577787T>C	GRCh38
NC_000006.11:g.577787T>C , CM000668.1:g.577787T>C	GRCh37
NC_000006.10:g.522787T>C	NCBI36
NG_047166.1:g.120355A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000230449.9:c.1193-905A>G MANE Select	ENSP00000230449.4:n.1193-905A>G
ENST00000230449.8:c.1193-905A>G	ENSP00000230449.4:n.1193-905A>G
NM_018303.5:c.1193-905A>G	NP_060773.3:n.1193-905A>G
NR_073064.1:n.1521-905A>G
XM_017011018.1:c.1193-905A>G	XP_016866507.1:n.1193-905A>G
XM_017011019.1:c.1193-905A>G	XP_016866508.1:n.1193-905A>G
XM_017011020.1:c.1193-905A>G	XP_016866509.1:n.1193-905A>G
XM_017011021.1:c.1193-905A>G	XP_016866510.1:n.1193-905A>G
XM_017011022.1:c.1193-905A>G	XP_016866511.1:n.1193-905A>G
XM_017011023.1:c.1193-905A>G	XP_016866512.1:n.1193-905A>G
XM_017011024.1:c.1193-905A>G	XP_016866513.1:n.1193-905A>G
XM_017011025.1:c.1193-905A>G	XP_016866514.1:n.1193-905A>G
XM_017011026.1:c.1193-905A>G	XP_016866515.1:n.1193-905A>G
NM_018303.6:c.1193-905A>G MANE Select	NP_060773.3:n.1193-905A>G
NR_073064.2:n.1519-905A>G