Canonical Allele Identifier: CA2580967605
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs7911129

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110581113A>T , CM000672.2:g.110581113A>T GRCh38
NC_000010.10:g.112340871A>T , CM000672.1:g.112340871A>T GRCh37
NC_000010.9:g.112330861A>T NCBI36
NG_012217.1:g.18423A>T , LRG_774:g.18423A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.680+92A>T
ENST00000687823.1:n.461+92A>T
ENST00000689932.1:n.2610+92A>T
ENST00000691297.1:n.680+92A>T
ENST00000691527.1:n.1350+92A>T
ENST00000692792.1:n.666+92A>T
ENST00000361804.5:c.547+92A>T MANE Select ENSP00000354720.5:n.547+92A>T
ENST00000361804.4:c.547+92A>T ENSP00000354720.4:n.547+92A>T
ENST00000462899.1:n.693+92A>T
NM_005445.3:c.547+92A>T , LRG_774t1:c.547+92A>T NP_005436.1:n.547+92A>T
NM_005445.4:c.547+92A>T MANE Select NP_005436.1:n.547+92A>T