Canonical Allele Identifier: CA91956849
Gene: SORCS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10937823

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.7478695C>T , CM000666.2:g.7478695C>T GRCh38
NC_000004.10:g.7531322C>T NCBI36
NC_000004.11:g.7480422C>T , CM000666.1:g.7480422C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000329016.10:c.33-52835C>T ENSP00000329124.10:p.=
ENST00000507866.6:c.549-52835C>T ENSP00000422185.2:p.=
ENST00000511199.1:n.164-52835C>T
NM_020777.2:n.549-52835C>T VV NP_065828.2:p.=
XM_005247987.3:c.549-52835C>T XP_005248044.2:p.=
XM_011513514.1:c.549-52835C>T XP_011511816.1:p.=
XM_011513515.1:c.549-52835C>T XP_011511817.1:p.=
XM_011513516.1:c.549-52835C>T XP_011511818.1:p.=
XM_011513517.1:c.156-52835C>T XP_011511819.1:p.=