Canonical Allele Identifier: CA2722792381
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861180128

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110589864T>G , CM000672.2:g.110589864T>G GRCh38
NC_000010.10:g.112349622T>G , CM000672.1:g.112349622T>G GRCh37
NC_000010.9:g.112339612T>G NCBI36
NG_012217.1:g.27174T>G , LRG_774:g.27174T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684797.1:n.1310-28T>G
ENST00000684988.1:n.2055-28T>G
ENST00000687823.1:n.1324-28T>G
ENST00000689932.1:n.3473-28T>G
ENST00000691297.1:n.1543-28T>G
ENST00000691527.1:n.2213-28T>G
ENST00000692792.1:n.1529-28T>G
ENST00000361804.5:c.1410-28T>G MANE Select ENSP00000354720.5:n.1410-28T>G
ENST00000361804.4:c.1410-28T>G ENSP00000354720.4:n.1410-28T>G
NM_005445.3:c.1410-28T>G , LRG_774t1:c.1410-28T>G NP_005436.1:n.1410-28T>G
NM_005445.4:c.1410-28T>G MANE Select NP_005436.1:n.1410-28T>G