Canonical Allele Identifier: CA378377259

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112341813T>G (hg19) ; chr10:g.110582055T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110582055T>G , CM000672.2:g.110582055T>G	GRCh38
NC_000010.10:g.112341813T>G , CM000672.1:g.112341813T>G	GRCh37
NC_000010.9:g.112331803T>G	NCBI36
NG_012217.1:g.19365T>G , LRG_774:g.19365T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.813T>G
ENST00000687823.1:n.594T>G
ENST00000689932.1:n.2743T>G
ENST00000691297.1:n.813T>G
ENST00000691527.1:n.1483T>G
ENST00000692792.1:n.799T>G
ENST00000361804.5:c.680T>G MANE Select	ENSP00000354720.5:p.Ile227Ser
ENST00000361804.4:c.680T>G	ENSP00000354720.4:p.Ile227Ser
NM_005445.3:c.680T>G , LRG_774t1:c.680T>G	NP_005436.1:p.Ile227Ser
NM_005445.4:c.680T>G MANE Select	NP_005436.1:p.Ile227Ser