Canonical Allele Identifier: CA378393374
Gene: SMC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310573
ClinVar RCV Id: RCV001767687
dbSNP Id: rs2134752521

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601644C>G , CM000672.2:g.110601644C>G GRCh38
NC_000010.10:g.112361402C>G , CM000672.1:g.112361402C>G GRCh37
NC_000010.9:g.112351392C>G NCBI36
NG_012217.1:g.38954C>G , LRG_774:g.38954C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4885C>G
ENST00000685743.1:n.2360C>G
ENST00000686057.1:n.1003C>G
ENST00000689321.1:n.1615C>G
ENST00000689986.1:n.441C>G
ENST00000361804.5:c.2652C>G MANE Select ENSP00000354720.5:p.Asp884Glu
ENST00000361804.4:c.2652C>G ENSP00000354720.4:p.Asp884Glu
NM_005445.3:c.2652C>G , LRG_774t1:c.2652C>G NP_005436.1:p.Asp884Glu
NM_005445.4:c.2652C>G MANE Select NP_005436.1:p.Asp884Glu