Canonical Allele Identifier: CA471370195

Gene: SMC3

Linked Data

• dbSNP Id: rs1860969562
• gnomAD v4: 10-110577492-A-G
• MyVariant Identifiers: chr10:g.112337250A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110577492A>G , CM000672.2:g.110577492A>G	GRCh38
NC_000010.10:g.112337250A>G , CM000672.1:g.112337250A>G	GRCh37
NC_000010.9:g.112327240A>G	NCBI36
NG_012217.1:g.14802A>G , LRG_774:g.14802A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684988.1:n.403A>G
ENST00000687823.1:n.184A>G
ENST00000689932.1:n.2333A>G
ENST00000691297.1:n.403A>G
ENST00000691527.1:n.360A>G
ENST00000692792.1:n.389A>G
ENST00000361804.5:c.270A>G MANE Select	ENSP00000354720.5:p.Pro90=
ENST00000361804.4:c.270A>G	ENSP00000354720.4:p.Pro90=
ENST00000462899.1:n.416A>G
NM_005445.3:c.270A>G , LRG_774t1:c.270A>G	NP_005436.1:p.Pro90=
NM_005445.4:c.270A>G MANE Select	NP_005436.1:p.Pro90=