Canonical Allele Identifier: CA595712630
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112337290T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110577532T>G , CM000672.2:g.110577532T>G GRCh38
NC_000010.10:g.112337290T>G , CM000672.1:g.112337290T>G GRCh37
NC_000010.9:g.112327280T>G NCBI36
NG_012217.1:g.14842T>G , LRG_774:g.14842T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.403+40T>G
ENST00000687823.1:n.184+40T>G
ENST00000689932.1:n.2333+40T>G
ENST00000691297.1:n.403+40T>G
ENST00000691527.1:n.360+40T>G
ENST00000692792.1:n.389+40T>G
ENST00000361804.5:c.270+40T>G MANE Select ENSP00000354720.5:n.270+40T>G
ENST00000361804.4:c.270+40T>G ENSP00000354720.4:n.270+40T>G
ENST00000462899.1:n.416+40T>G
NM_005445.3:c.270+40T>G , LRG_774t1:c.270+40T>G NP_005436.1:n.270+40T>G
NM_005445.4:c.270+40T>G MANE Select NP_005436.1:n.270+40T>G