Canonical Allele Identifier: CA932511792
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1182285160

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110577383A>T , CM000672.2:g.110577383A>T GRCh38
NC_000010.10:g.112337141A>T , CM000672.1:g.112337141A>T GRCh37
NC_000010.9:g.112327131A>T NCBI36
NG_012217.1:g.14693A>T , LRG_774:g.14693A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.332-38A>T
ENST00000687823.1:n.113-38A>T
ENST00000689932.1:n.2262-38A>T
ENST00000691297.1:n.332-38A>T
ENST00000691527.1:n.289-38A>T
ENST00000692792.1:n.318-38A>T
ENST00000361804.5:c.199-38A>T MANE Select ENSP00000354720.5:n.199-38A>T
ENST00000361804.4:c.199-38A>T ENSP00000354720.4:n.199-38A>T
ENST00000462899.1:n.345-38A>T
NM_005445.3:c.199-38A>T , LRG_774t1:c.199-38A>T NP_005436.1:n.199-38A>T
NM_005445.4:c.199-38A>T MANE Select NP_005436.1:n.199-38A>T