Canonical Allele Identifier: CA471506141

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112361747C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110601989C>T , CM000672.2:g.110601989C>T	GRCh38
NC_000010.10:g.112361747C>T , CM000672.1:g.112361747C>T	GRCh37
NC_000010.9:g.112351737C>T	NCBI36
NG_012217.1:g.39299C>T , LRG_774:g.39299C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.5149C>T
ENST00000685743.1:n.2624C>T
ENST00000686057.1:n.1267C>T
ENST00000689321.1:n.1879C>T
ENST00000689986.1:n.705C>T
ENST00000361804.5:c.2916C>T MANE Select	ENSP00000354720.5:p.Cys972=
ENST00000361804.4:c.2916C>T	ENSP00000354720.4:p.Cys972=
NM_005445.3:c.2916C>T , LRG_774t1:c.2916C>T	NP_005436.1:p.Cys972=
NM_005445.4:c.2916C>T MANE Select	NP_005436.1:p.Cys972=