Canonical Allele Identifier: CA2610887876
Gene: SMC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110573853T>A , CM000672.2:g.110573853T>A GRCh38
NC_000010.10:g.112333611T>A , CM000672.1:g.112333611T>A GRCh37
NC_000010.9:g.112323601T>A NCBI36
NG_012217.1:g.11163T>A , LRG_774:g.11163T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.263+108T>A
ENST00000687823.1:n.45-1483T>A
ENST00000689932.1:n.711T>A
ENST00000691297.1:n.263+108T>A
ENST00000691527.1:n.220+108T>A
ENST00000692792.1:n.249+108T>A
ENST00000361804.5:c.130+108T>A MANE Select ENSP00000354720.5:n.130+108T>A
ENST00000361804.4:c.130+108T>A ENSP00000354720.4:n.130+108T>A
ENST00000462899.1:n.276+108T>A
NM_005445.3:c.130+108T>A , LRG_774t1:c.130+108T>A NP_005436.1:n.130+108T>A
NM_005445.4:c.130+108T>A MANE Select NP_005436.1:n.130+108T>A