Canonical Allele Identifier: CA798425821

Gene: SORCS2

Linked Data

• dbSNP Id: rs1211599510
• gnomAD v3: 4-7478643-G-A
• gnomAD v4: 4-7478643-G-A
• MyVariant Identifiers: chr4:g.7480370G>A (hg19) ; chr4:g.7478643G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.7478643G>A , CM000666.2:g.7478643G>A	GRCh38
NC_000004.11:g.7480370G>A , CM000666.1:g.7480370G>A	GRCh37
NC_000004.10:g.7531270G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329016.10:c.33-52887G>A	ENSP00000329124.10:n.33-52887G>A
ENST00000507866.6:c.549-52887G>A MANE Select	ENSP00000422185.2:n.549-52887G>A
ENST00000511199.1:n.164-52887G>A
NM_020777.2:c.549-52887G>A	NP_065828.2:n.549-52887G>A
XM_005247987.3:c.549-52887G>A	XP_005248044.2:n.549-52887G>A
XM_011513514.1:c.549-52887G>A	XP_011511816.1:n.549-52887G>A
XM_011513515.1:c.549-52887G>A	XP_011511817.1:n.549-52887G>A
XM_011513516.1:c.549-52887G>A	XP_011511818.1:n.549-52887G>A
XM_011513517.1:c.156-52887G>A	XP_011511819.1:n.156-52887G>A
XM_005247987.4:c.549-52887G>A	XP_005248044.2:n.549-52887G>A
XM_011513514.2:c.549-52887G>A	XP_011511816.1:n.549-52887G>A
XM_011513515.2:c.549-52887G>A	XP_011511817.1:n.549-52887G>A
XM_011513516.2:c.549-52887G>A	XP_011511818.1:n.549-52887G>A
XM_017008481.1:c.549-52887G>A	XP_016863970.1:n.549-52887G>A
NM_020777.3:c.549-52887G>A MANE Select	NP_065828.2:n.549-52887G>A