Canonical Allele Identifier: CA378369905

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112335121T>A (hg19) ; chr10:g.110575363T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110575363T>A , CM000672.2:g.110575363T>A	GRCh38
NC_000010.10:g.112335121T>A , CM000672.1:g.112335121T>A	GRCh37
NC_000010.9:g.112325111T>A	NCBI36
NG_012217.1:g.12673T>A , LRG_774:g.12673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.291T>A
ENST00000687823.1:n.72T>A
ENST00000689932.1:n.2221T>A
ENST00000691297.1:n.291T>A
ENST00000691527.1:n.248T>A
ENST00000692792.1:n.277T>A
ENST00000361804.5:c.158T>A MANE Select	ENSP00000354720.5:p.Phe53Tyr
ENST00000361804.4:c.158T>A	ENSP00000354720.4:p.Phe53Tyr
ENST00000462899.1:n.304T>A
NM_005445.3:c.158T>A , LRG_774t1:c.158T>A	NP_005436.1:p.Phe53Tyr
NM_005445.4:c.158T>A MANE Select	NP_005436.1:p.Phe53Tyr