Canonical Allele Identifier: CA2722991439
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs2134724419

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110581765T>C , CM000672.2:g.110581765T>C GRCh38
NC_000010.10:g.112341523T>C , CM000672.1:g.112341523T>C GRCh37
NC_000010.9:g.112331513T>C NCBI36
NG_012217.1:g.19075T>C , LRG_774:g.19075T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.681-158T>C
ENST00000687823.1:n.462-158T>C
ENST00000689932.1:n.2611-158T>C
ENST00000691297.1:n.681-158T>C
ENST00000691527.1:n.1351-158T>C
ENST00000692792.1:n.667-158T>C
ENST00000361804.5:c.548-158T>C MANE Select ENSP00000354720.5:n.548-158T>C
ENST00000361804.4:c.548-158T>C ENSP00000354720.4:n.548-158T>C
ENST00000462899.1:n.694-158T>C
NM_005445.3:c.548-158T>C , LRG_774t1:c.548-158T>C NP_005436.1:n.548-158T>C
NM_005445.4:c.548-158T>C MANE Select NP_005436.1:n.548-158T>C