Canonical Allele Identifier: CA659257923
Gene: SORCS3 HGNC NCBI

Linked Data

dbSNP Id: rs1404895461
gnomAD v3: 10-104850193-G-T
gnomAD v4: 10-104850193-G-T
MyVariant Identifiers: chr10:g.106609951G>T (hg19) chr10:g.104850193G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104850193G>T , CM000672.2:g.104850193G>T GRCh38
NC_000010.10:g.106609951G>T , CM000672.1:g.106609951G>T GRCh37
NC_000010.9:g.106599941G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369701.8:c.695+7334G>T MANE Select ENSP00000358715.3:n.695+7334G>T
ENST00000369699.8:c.695+7334G>T ENSP00000358713.5:n.695+7334G>T
ENST00000369701.7:c.695+7334G>T ENSP00000358715.3:n.695+7334G>T
NM_014978.2:c.695+7334G>T NP_055793.1:n.695+7334G>T
XM_011539541.1:c.695+7334G>T XP_011537843.1:n.695+7334G>T
NM_014978.3:c.695+7334G>T MANE Select NP_055793.1:n.695+7334G>T
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