Canonical Allele Identifier: CA378376296

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112341765C>A (hg19) ; chr10:g.110582007C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110582007C>A , CM000672.2:g.110582007C>A	GRCh38
NC_000010.10:g.112341765C>A , CM000672.1:g.112341765C>A	GRCh37
NC_000010.9:g.112331755C>A	NCBI36
NG_012217.1:g.19317C>A , LRG_774:g.19317C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.765C>A
ENST00000687823.1:n.546C>A
ENST00000689932.1:n.2695C>A
ENST00000691297.1:n.765C>A
ENST00000691527.1:n.1435C>A
ENST00000692792.1:n.751C>A
ENST00000361804.5:c.632C>A MANE Select	ENSP00000354720.5:p.Ala211Asp
ENST00000361804.4:c.632C>A	ENSP00000354720.4:p.Ala211Asp
NM_005445.3:c.632C>A , LRG_774t1:c.632C>A	NP_005436.1:p.Ala211Asp
NM_005445.4:c.632C>A MANE Select	NP_005436.1:p.Ala211Asp