Canonical Allele Identifier: CA378372056

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112337245T>G (hg19) ; chr10:g.110577487T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110577487T>G , CM000672.2:g.110577487T>G	GRCh38
NC_000010.10:g.112337245T>G , CM000672.1:g.112337245T>G	GRCh37
NC_000010.9:g.112327235T>G	NCBI36
NG_012217.1:g.14797T>G , LRG_774:g.14797T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684988.1:n.398T>G
ENST00000687823.1:n.179T>G
ENST00000689932.1:n.2328T>G
ENST00000691297.1:n.398T>G
ENST00000691527.1:n.355T>G
ENST00000692792.1:n.384T>G
ENST00000361804.5:c.265T>G MANE Select	ENSP00000354720.5:p.Leu89Val
ENST00000361804.4:c.265T>G	ENSP00000354720.4:p.Leu89Val
ENST00000462899.1:n.411T>G
NM_005445.3:c.265T>G , LRG_774t1:c.265T>G	NP_005436.1:p.Leu89Val
NM_005445.4:c.265T>G MANE Select	NP_005436.1:p.Leu89Val