Canonical Allele Identifier: CA378369297

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112333476G>T (hg19) ; chr10:g.110573718G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110573718G>T , CM000672.2:g.110573718G>T	GRCh38
NC_000010.10:g.112333476G>T , CM000672.1:g.112333476G>T	GRCh37
NC_000010.9:g.112323466G>T	NCBI36
NG_012217.1:g.11028G>T , LRG_774:g.11028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.236G>T
ENST00000687823.1:n.45-1618G>T
ENST00000689932.1:n.576G>T
ENST00000691297.1:n.236G>T
ENST00000691527.1:n.193G>T
ENST00000692792.1:n.222G>T
ENST00000361804.5:c.103G>T MANE Select	ENSP00000354720.5:p.Gly35Ter
ENST00000361804.4:c.103G>T	ENSP00000354720.4:p.Gly35Ter
ENST00000462899.1:n.249G>T
NM_005445.3:c.103G>T , LRG_774t1:c.103G>T	NP_005436.1:p.Gly35Ter
NM_005445.4:c.103G>T MANE Select	NP_005436.1:p.Gly35Ter