Canonical Allele Identifier: CA378376427

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112341791A>G (hg19) ; chr10:g.110582033A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110582033A>G , CM000672.2:g.110582033A>G	GRCh38
NC_000010.10:g.112341791A>G , CM000672.1:g.112341791A>G	GRCh37
NC_000010.9:g.112331781A>G	NCBI36
NG_012217.1:g.19343A>G , LRG_774:g.19343A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.791A>G
ENST00000687823.1:n.572A>G
ENST00000689932.1:n.2721A>G
ENST00000691297.1:n.791A>G
ENST00000691527.1:n.1461A>G
ENST00000692792.1:n.777A>G
ENST00000361804.5:c.658A>G MANE Select	ENSP00000354720.5:p.Arg220Gly
ENST00000361804.4:c.658A>G	ENSP00000354720.4:p.Arg220Gly
NM_005445.3:c.658A>G , LRG_774t1:c.658A>G	NP_005436.1:p.Arg220Gly
NM_005445.4:c.658A>G MANE Select	NP_005436.1:p.Arg220Gly