Canonical Allele Identifier: CA5688311
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs761995373
COSMIC: COSM914747

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601973G>A , CM000672.2:g.110601973G>A GRCh38
NC_000010.10:g.112361731G>A , CM000672.1:g.112361731G>A GRCh37
NC_000010.9:g.112351721G>A NCBI36
NG_012217.1:g.39283G>A , LRG_774:g.39283G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5133G>A
ENST00000685743.1:n.2608G>A
ENST00000686057.1:n.1251G>A
ENST00000689321.1:n.1863G>A
ENST00000689986.1:n.689G>A
ENST00000361804.5:c.2900G>A MANE Select ENSP00000354720.5:p.Arg967Gln
ENST00000361804.4:c.2900G>A ENSP00000354720.4:p.Arg967Gln
NM_005445.3:c.2900G>A , LRG_774t1:c.2900G>A NP_005436.1:p.Arg967Gln
NM_005445.4:c.2900G>A MANE Select NP_005436.1:p.Arg967Gln