Canonical Allele Identifier: CA378369456

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112333496T>A (hg19) ; chr10:g.110573738T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110573738T>A , CM000672.2:g.110573738T>A	GRCh38
NC_000010.10:g.112333496T>A , CM000672.1:g.112333496T>A	GRCh37
NC_000010.9:g.112323486T>A	NCBI36
NG_012217.1:g.11048T>A , LRG_774:g.11048T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.256T>A
ENST00000687823.1:n.45-1598T>A
ENST00000689932.1:n.596T>A
ENST00000691297.1:n.256T>A
ENST00000691527.1:n.213T>A
ENST00000692792.1:n.242T>A
ENST00000361804.5:c.123T>A MANE Select	ENSP00000354720.5:p.Phe41Leu
ENST00000361804.4:c.123T>A	ENSP00000354720.4:p.Phe41Leu
ENST00000462899.1:n.269T>A
NM_005445.3:c.123T>A , LRG_774t1:c.123T>A	NP_005436.1:p.Phe41Leu
NM_005445.4:c.123T>A MANE Select	NP_005436.1:p.Phe41Leu