Canonical Allele Identifier: CA91956878

Gene: SORCS2

Linked Data

• dbSNP Id: rs866461535
• MyVariant Identifiers: chr4:g.7480490T>C (hg19) ; chr4:g.7478763T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.7478763T>C , CM000666.2:g.7478763T>C	GRCh38
NC_000004.11:g.7480490T>C , CM000666.1:g.7480490T>C	GRCh37
NC_000004.10:g.7531390T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329016.10:c.33-52767T>C	ENSP00000329124.10:n.33-52767T>C
ENST00000507866.6:c.549-52767T>C MANE Select	ENSP00000422185.2:n.549-52767T>C
ENST00000511199.1:n.164-52767T>C
NM_020777.2:c.549-52767T>C	NP_065828.2:n.549-52767T>C
XM_005247987.3:c.549-52767T>C	XP_005248044.2:n.549-52767T>C
XM_011513514.1:c.549-52767T>C	XP_011511816.1:n.549-52767T>C
XM_011513515.1:c.549-52767T>C	XP_011511817.1:n.549-52767T>C
XM_011513516.1:c.549-52767T>C	XP_011511818.1:n.549-52767T>C
XM_011513517.1:c.156-52767T>C	XP_011511819.1:n.156-52767T>C
XM_005247987.4:c.549-52767T>C	XP_005248044.2:n.549-52767T>C
XM_011513514.2:c.549-52767T>C	XP_011511816.1:n.549-52767T>C
XM_011513515.2:c.549-52767T>C	XP_011511817.1:n.549-52767T>C
XM_011513516.2:c.549-52767T>C	XP_011511818.1:n.549-52767T>C
XM_017008481.1:c.549-52767T>C	XP_016863970.1:n.549-52767T>C
NM_020777.3:c.549-52767T>C MANE Select	NP_065828.2:n.549-52767T>C