Canonical Allele Identifier: CA378393594
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861389818

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601735A>G , CM000672.2:g.110601735A>G GRCh38
NC_000010.10:g.112361493A>G , CM000672.1:g.112361493A>G GRCh37
NC_000010.9:g.112351483A>G NCBI36
NG_012217.1:g.39045A>G , LRG_774:g.39045A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.4976A>G
ENST00000685743.1:n.2451A>G
ENST00000686057.1:n.1094A>G
ENST00000689321.1:n.1706A>G
ENST00000689986.1:n.532A>G
ENST00000361804.5:c.2743A>G MANE Select ENSP00000354720.5:p.Ile915Val
ENST00000361804.4:c.2743A>G ENSP00000354720.4:p.Ile915Val
NM_005445.3:c.2743A>G , LRG_774t1:c.2743A>G NP_005436.1:p.Ile915Val
NM_005445.4:c.2743A>G MANE Select NP_005436.1:p.Ile915Val