Canonical Allele Identifier: CA92322953

Gene: SORCS2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.7218206T>A , CM000666.2:g.7218206T>A	GRCh38
NC_000004.11:g.7219933T>A , CM000666.1:g.7219933T>A	GRCh37
NC_000004.10:g.7270834T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507866.6:c.480+25080T>A MANE Select	ENSP00000422185.2:n.480+25080T>A
NM_020777.2:c.480+25080T>A	NP_065828.2:n.480+25080T>A
XM_005247987.3:c.480+25080T>A	XP_005248044.2:n.480+25080T>A
XM_011513514.1:c.480+25080T>A	XP_011511816.1:n.480+25080T>A
XM_011513515.1:c.480+25080T>A	XP_011511817.1:n.480+25080T>A
XM_011513516.1:c.480+25080T>A	XP_011511818.1:n.480+25080T>A
XM_005247987.4:c.480+25080T>A	XP_005248044.2:n.480+25080T>A
XM_011513514.2:c.480+25080T>A	XP_011511816.1:n.480+25080T>A
XM_011513515.2:c.480+25080T>A	XP_011511817.1:n.480+25080T>A
XM_011513516.2:c.480+25080T>A	XP_011511818.1:n.480+25080T>A
XM_017008481.1:c.480+25080T>A	XP_016863970.1:n.480+25080T>A
NM_020777.3:c.480+25080T>A MANE Select	NP_065828.2:n.480+25080T>A