Canonical Allele Identifier: CA212800935
Gene: SORCS3 HGNC NCBI

Linked Data

dbSNP Id: rs973498725
gnomAD v3: 10-104850108-A-C
gnomAD v4: 10-104850108-A-C
MyVariant Identifiers: chr10:g.106609866A>C (hg19) chr10:g.104850108A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104850108A>C , CM000672.2:g.104850108A>C GRCh38
NC_000010.10:g.106609866A>C , CM000672.1:g.106609866A>C GRCh37
NC_000010.9:g.106599856A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369701.8:c.695+7249A>C MANE Select ENSP00000358715.3:n.695+7249A>C
ENST00000369699.8:c.695+7249A>C ENSP00000358713.5:n.695+7249A>C
ENST00000369701.7:c.695+7249A>C ENSP00000358715.3:n.695+7249A>C
NM_014978.2:c.695+7249A>C NP_055793.1:n.695+7249A>C
XM_011539541.1:c.695+7249A>C XP_011537843.1:n.695+7249A>C
NM_014978.3:c.695+7249A>C MANE Select NP_055793.1:n.695+7249A>C
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