Canonical Allele Identifier: CA378393444

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112361433A>G (hg19) ; chr10:g.110601675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110601675A>G , CM000672.2:g.110601675A>G	GRCh38
NC_000010.10:g.112361433A>G , CM000672.1:g.112361433A>G	GRCh37
NC_000010.9:g.112351423A>G	NCBI36
NG_012217.1:g.38985A>G , LRG_774:g.38985A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.4916A>G
ENST00000685743.1:n.2391A>G
ENST00000686057.1:n.1034A>G
ENST00000689321.1:n.1646A>G
ENST00000689986.1:n.472A>G
ENST00000361804.5:c.2683A>G MANE Select	ENSP00000354720.5:p.Lys895Glu
ENST00000361804.4:c.2683A>G	ENSP00000354720.4:p.Lys895Glu
NM_005445.3:c.2683A>G , LRG_774t1:c.2683A>G	NP_005436.1:p.Lys895Glu
NM_005445.4:c.2683A>G MANE Select	NP_005436.1:p.Lys895Glu