Canonical Allele Identifier: CA378387927

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112349699A>G (hg19) ; chr10:g.110589941A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110589941A>G , CM000672.2:g.110589941A>G	GRCh38
NC_000010.10:g.112349699A>G , CM000672.1:g.112349699A>G	GRCh37
NC_000010.9:g.112339689A>G	NCBI36
NG_012217.1:g.27251A>G , LRG_774:g.27251A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684797.1:n.1359A>G
ENST00000684988.1:n.2104A>G
ENST00000687823.1:n.1373A>G
ENST00000689932.1:n.3522A>G
ENST00000691297.1:n.1592A>G
ENST00000691527.1:n.2262A>G
ENST00000692792.1:n.1578A>G
ENST00000361804.5:c.1459A>G MANE Select	ENSP00000354720.5:p.Arg487Gly
ENST00000361804.4:c.1459A>G	ENSP00000354720.4:p.Arg487Gly
NM_005445.3:c.1459A>G , LRG_774t1:c.1459A>G	NP_005436.1:p.Arg487Gly
NM_005445.4:c.1459A>G MANE Select	NP_005436.1:p.Arg487Gly