Canonical Allele Identifier: CA378387903

Gene: SMC3

Linked Data

• gnomAD v4: 10-110589938-A-G
• MyVariant Identifiers: chr10:g.112349696A>G (hg19) ; chr10:g.110589938A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110589938A>G , CM000672.2:g.110589938A>G	GRCh38
NC_000010.10:g.112349696A>G , CM000672.1:g.112349696A>G	GRCh37
NC_000010.9:g.112339686A>G	NCBI36
NG_012217.1:g.27248A>G , LRG_774:g.27248A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684797.1:n.1356A>G
ENST00000684988.1:n.2101A>G
ENST00000687823.1:n.1370A>G
ENST00000689932.1:n.3519A>G
ENST00000691297.1:n.1589A>G
ENST00000691527.1:n.2259A>G
ENST00000692792.1:n.1575A>G
ENST00000361804.5:c.1456A>G MANE Select	ENSP00000354720.5:p.Lys486Glu
ENST00000361804.4:c.1456A>G	ENSP00000354720.4:p.Lys486Glu
NM_005445.3:c.1456A>G , LRG_774t1:c.1456A>G	NP_005436.1:p.Lys486Glu
NM_005445.4:c.1456A>G MANE Select	NP_005436.1:p.Lys486Glu