Canonical Allele Identifier: CA2722794123
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1860992521
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578799G>A , CM000672.2:g.110578799G>A GRCh38
NC_000010.10:g.112338557G>A , CM000672.1:g.112338557G>A GRCh37
NC_000010.9:g.112328547G>A NCBI36
NG_012217.1:g.16109G>A , LRG_774:g.16109G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.562+93G>A
ENST00000687823.1:n.343+93G>A
ENST00000689932.1:n.2492+93G>A
ENST00000691297.1:n.562+93G>A
ENST00000691527.1:n.1232+93G>A
ENST00000692792.1:n.548+93G>A
ENST00000361804.5:c.429+93G>A MANE Select ENSP00000354720.5:n.429+93G>A
ENST00000361804.4:c.429+93G>A ENSP00000354720.4:n.429+93G>A
ENST00000462899.1:n.575+93G>A
NM_005445.3:c.429+93G>A , LRG_774t1:c.429+93G>A NP_005436.1:n.429+93G>A
NM_005445.4:c.429+93G>A MANE Select NP_005436.1:n.429+93G>A
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