Canonical Allele Identifier: CA378393804
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861390672

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601820T>C , CM000672.2:g.110601820T>C GRCh38
NC_000010.10:g.112361578T>C , CM000672.1:g.112361578T>C GRCh37
NC_000010.9:g.112351568T>C NCBI36
NG_012217.1:g.39130T>C , LRG_774:g.39130T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5061T>C
ENST00000685743.1:n.2536T>C
ENST00000686057.1:n.1179T>C
ENST00000689321.1:n.1791T>C
ENST00000689986.1:n.617T>C
ENST00000361804.5:c.2828T>C MANE Select ENSP00000354720.5:p.Ile943Thr
ENST00000361804.4:c.2828T>C ENSP00000354720.4:p.Ile943Thr
NM_005445.3:c.2828T>C , LRG_774t1:c.2828T>C NP_005436.1:p.Ile943Thr
NM_005445.4:c.2828T>C MANE Select NP_005436.1:p.Ile943Thr