Canonical Allele Identifier: CA814057598

Gene: SV2C

Linked Data

• dbSNP Id: rs1338181788
• gnomAD v3: 5-76143429-G-A
• gnomAD v4: 5-76143429-G-A
• MyVariant Identifiers: chr5:g.75439254G>A (hg19) ; chr5:g.76143429G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76143429G>A , CM000667.2:g.76143429G>A	GRCh38
NC_000005.9:g.75439254G>A , CM000667.1:g.75439254G>A	GRCh37
NC_000005.8:g.75475010G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502798.7:c.580+11099G>A MANE Select	ENSP00000423541.2:n.580+11099G>A
ENST00000322285.7:c.580+11099G>A	ENSP00000316983.7:n.580+11099G>A
ENST00000502798.6:c.580+11099G>A	ENSP00000423541.2:n.580+11099G>A
NM_001297716.1:c.580+11099G>A	NP_001284645.1:n.580+11099G>A
NM_014979.3:c.580+11099G>A	NP_055794.3:n.580+11099G>A
XM_011543281.1:c.580+11099G>A	XP_011541583.1:n.580+11099G>A
XM_011543282.1:c.8+11099G>A	XP_011541584.1:n.8+11099G>A
XM_011543281.3:c.580+11099G>A	XP_011541583.1:n.580+11099G>A
XM_011543282.3:c.580+11099G>A	XP_011541584.2:n.580+11099G>A
NM_014979.4:c.580+11099G>A MANE Select	NP_055794.3:n.580+11099G>A
NM_001297716.2:c.580+11099G>A	NP_001284645.1:n.580+11099G>A