Canonical Allele Identifier: CA378393784
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs2134752709

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601813A>C , CM000672.2:g.110601813A>C GRCh38
NC_000010.10:g.112361571A>C , CM000672.1:g.112361571A>C GRCh37
NC_000010.9:g.112351561A>C NCBI36
NG_012217.1:g.39123A>C , LRG_774:g.39123A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5054A>C
ENST00000685743.1:n.2529A>C
ENST00000686057.1:n.1172A>C
ENST00000689321.1:n.1784A>C
ENST00000689986.1:n.610A>C
ENST00000361804.5:c.2821A>C MANE Select ENSP00000354720.5:p.Lys941Gln
ENST00000361804.4:c.2821A>C ENSP00000354720.4:p.Lys941Gln
NM_005445.3:c.2821A>C , LRG_774t1:c.2821A>C NP_005436.1:p.Lys941Gln
NM_005445.4:c.2821A>C MANE Select NP_005436.1:p.Lys941Gln