Canonical Allele Identifier: CA213229024

Gene: SMC3

Linked Data

• dbSNP Id: rs910984772
• gnomAD v3: 10-110578813-C-G
• gnomAD v4: 10-110578813-C-G
• MyVariant Identifiers: chr10:g.112338571C>G (hg19) ; chr10:g.110578813C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110578813C>G , CM000672.2:g.110578813C>G	GRCh38
NC_000010.10:g.112338571C>G , CM000672.1:g.112338571C>G	GRCh37
NC_000010.9:g.112328561C>G	NCBI36
NG_012217.1:g.16123C>G , LRG_774:g.16123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.562+107C>G
ENST00000687823.1:n.343+107C>G
ENST00000689932.1:n.2492+107C>G
ENST00000691297.1:n.562+107C>G
ENST00000691527.1:n.1232+107C>G
ENST00000692792.1:n.548+107C>G
ENST00000361804.5:c.429+107C>G MANE Select	ENSP00000354720.5:n.429+107C>G
ENST00000361804.4:c.429+107C>G	ENSP00000354720.4:n.429+107C>G
ENST00000462899.1:n.575+107C>G
NM_005445.3:c.429+107C>G , LRG_774t1:c.429+107C>G	NP_005436.1:n.429+107C>G
NM_005445.4:c.429+107C>G MANE Select	NP_005436.1:n.429+107C>G