Canonical Allele Identifier: CA595712939
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs955684370

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578549A>G , CM000672.2:g.110578549A>G GRCh38
NC_000010.10:g.112338307A>G , CM000672.1:g.112338307A>G GRCh37
NC_000010.9:g.112328297A>G NCBI36
NG_012217.1:g.15859A>G , LRG_774:g.15859A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.484-79A>G
ENST00000687823.1:n.265-79A>G
ENST00000689932.1:n.2414-79A>G
ENST00000691297.1:n.484-79A>G
ENST00000691527.1:n.1075A>G
ENST00000692792.1:n.470-79A>G
ENST00000361804.5:c.351-79A>G MANE Select ENSP00000354720.5:n.351-79A>G
ENST00000361804.4:c.351-79A>G ENSP00000354720.4:n.351-79A>G
ENST00000462899.1:n.497-79A>G
NM_005445.3:c.351-79A>G , LRG_774t1:c.351-79A>G NP_005436.1:n.351-79A>G
NM_005445.4:c.351-79A>G MANE Select NP_005436.1:n.351-79A>G