Canonical Allele Identifier: CA826198000

Gene: EXOC2

Linked Data

• dbSNP Id: rs1290293637
• MyVariant Identifiers: chr6:g.577764A>G (hg19) ; chr6:g.577764A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.577764A>G , CM000668.2:g.577764A>G	GRCh38
NC_000006.11:g.577764A>G , CM000668.1:g.577764A>G	GRCh37
NC_000006.10:g.522764A>G	NCBI36
NG_047166.1:g.120378T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000230449.9:c.1193-882T>C MANE Select	ENSP00000230449.4:n.1193-882T>C
ENST00000230449.8:c.1193-882T>C	ENSP00000230449.4:n.1193-882T>C
NM_018303.5:c.1193-882T>C	NP_060773.3:n.1193-882T>C
NR_073064.1:n.1521-882T>C
XM_017011018.1:c.1193-882T>C	XP_016866507.1:n.1193-882T>C
XM_017011019.1:c.1193-882T>C	XP_016866508.1:n.1193-882T>C
XM_017011020.1:c.1193-882T>C	XP_016866509.1:n.1193-882T>C
XM_017011021.1:c.1193-882T>C	XP_016866510.1:n.1193-882T>C
XM_017011022.1:c.1193-882T>C	XP_016866511.1:n.1193-882T>C
XM_017011023.1:c.1193-882T>C	XP_016866512.1:n.1193-882T>C
XM_017011024.1:c.1193-882T>C	XP_016866513.1:n.1193-882T>C
XM_017011025.1:c.1193-882T>C	XP_016866514.1:n.1193-882T>C
XM_017011026.1:c.1193-882T>C	XP_016866515.1:n.1193-882T>C
NM_018303.6:c.1193-882T>C MANE Select	NP_060773.3:n.1193-882T>C
NR_073064.2:n.1519-882T>C