Canonical Allele Identifier: CA378388086

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112349718A>T (hg19) ; chr10:g.110589960A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110589960A>T , CM000672.2:g.110589960A>T	GRCh38
NC_000010.10:g.112349718A>T , CM000672.1:g.112349718A>T	GRCh37
NC_000010.9:g.112339708A>T	NCBI36
NG_012217.1:g.27270A>T , LRG_774:g.27270A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684797.1:n.1378A>T
ENST00000684988.1:n.2123A>T
ENST00000687823.1:n.1392A>T
ENST00000689932.1:n.3541A>T
ENST00000691297.1:n.1611A>T
ENST00000691527.1:n.2281A>T
ENST00000692792.1:n.1597A>T
ENST00000361804.5:c.1478A>T MANE Select	ENSP00000354720.5:p.Lys493Met
ENST00000361804.4:c.1478A>T	ENSP00000354720.4:p.Lys493Met
NM_005445.3:c.1478A>T , LRG_774t1:c.1478A>T	NP_005436.1:p.Lys493Met
NM_005445.4:c.1478A>T MANE Select	NP_005436.1:p.Lys493Met