Canonical Allele Identifier: CA2610884160

Gene: SMC3

Linked Data

• dbSNP Id: rs2134720652
• gnomAD v4: 10-110578788-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110578789dup , CM000672.2:g.110578789dup	GRCh38
NC_000010.10:g.112338547dup , CM000672.1:g.112338547dup	GRCh37
NC_000010.9:g.112328537dup	NCBI36
NG_012217.1:g.16099dup , LRG_774:g.16099dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.562+83dup
ENST00000687823.1:n.343+83dup
ENST00000689932.1:n.2492+83dup
ENST00000691297.1:n.562+83dup
ENST00000691527.1:n.1232+83dup
ENST00000692792.1:n.548+83dup
ENST00000361804.5:c.429+83dup MANE Select	ENSP00000354720.5:n.429+83dup
ENST00000361804.4:c.429+83dup	ENSP00000354720.4:n.429+83dup
ENST00000462899.1:n.575+83dup
NM_005445.3:c.429+83dup , LRG_774t1:c.429+83dup	NP_005436.1:n.429+83dup
NM_005445.4:c.429+83dup MANE Select	NP_005436.1:n.429+83dup