Canonical Allele Identifier: CA471368013

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112333487A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110573729A>G , CM000672.2:g.110573729A>G	GRCh38
NC_000010.10:g.112333487A>G , CM000672.1:g.112333487A>G	GRCh37
NC_000010.9:g.112323477A>G	NCBI36
NG_012217.1:g.11039A>G , LRG_774:g.11039A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.247A>G
ENST00000687823.1:n.45-1607A>G
ENST00000689932.1:n.587A>G
ENST00000691297.1:n.247A>G
ENST00000691527.1:n.204A>G
ENST00000692792.1:n.233A>G
ENST00000361804.5:c.114A>G MANE Select	ENSP00000354720.5:p.Lys38=
ENST00000361804.4:c.114A>G	ENSP00000354720.4:p.Lys38=
ENST00000462899.1:n.260A>G
NM_005445.3:c.114A>G , LRG_774t1:c.114A>G	NP_005436.1:p.Lys38=
NM_005445.4:c.114A>G MANE Select	NP_005436.1:p.Lys38=