Canonical Allele Identifier: CA5687789
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs781478694

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110582073A>G , CM000672.2:g.110582073A>G GRCh38
NC_000010.10:g.112341831A>G , CM000672.1:g.112341831A>G GRCh37
NC_000010.9:g.112331821A>G NCBI36
NG_012217.1:g.19383A>G , LRG_774:g.19383A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.831A>G
ENST00000687823.1:n.612A>G
ENST00000689932.1:n.2761A>G
ENST00000691297.1:n.831A>G
ENST00000691527.1:n.1501A>G
ENST00000692792.1:n.817A>G
ENST00000361804.5:c.698A>G MANE Select ENSP00000354720.5:p.Asn233Ser
ENST00000361804.4:c.698A>G ENSP00000354720.4:p.Asn233Ser
NM_005445.3:c.698A>G , LRG_774t1:c.698A>G NP_005436.1:p.Asn233Ser
NM_005445.4:c.698A>G MANE Select NP_005436.1:p.Asn233Ser