Canonical Allele Identifier: CA471368011

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112333484A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110573726A>G , CM000672.2:g.110573726A>G	GRCh38
NC_000010.10:g.112333484A>G , CM000672.1:g.112333484A>G	GRCh37
NC_000010.9:g.112323474A>G	NCBI36
NG_012217.1:g.11036A>G , LRG_774:g.11036A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.244A>G
ENST00000687823.1:n.45-1610A>G
ENST00000689932.1:n.584A>G
ENST00000691297.1:n.244A>G
ENST00000691527.1:n.201A>G
ENST00000692792.1:n.230A>G
ENST00000361804.5:c.111A>G MANE Select	ENSP00000354720.5:p.Gly37=
ENST00000361804.4:c.111A>G	ENSP00000354720.4:p.Gly37=
ENST00000462899.1:n.257A>G
NM_005445.3:c.111A>G , LRG_774t1:c.111A>G	NP_005436.1:p.Gly37=
NM_005445.4:c.111A>G MANE Select	NP_005436.1:p.Gly37=