Canonical Allele Identifier: CA378394449
Gene: SMC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602170T>A , CM000672.2:g.110602170T>A GRCh38
NC_000010.10:g.112361928T>A , CM000672.1:g.112361928T>A GRCh37
NC_000010.9:g.112351918T>A NCBI36
NG_012217.1:g.39480T>A , LRG_774:g.39480T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5330T>A
ENST00000685743.1:n.2805T>A
ENST00000686057.1:n.1448T>A
ENST00000689321.1:n.2060T>A
ENST00000689986.1:n.886T>A
ENST00000361804.5:c.3097T>A MANE Select ENSP00000354720.5:p.Phe1033Ile
ENST00000361804.4:c.3097T>A ENSP00000354720.4:p.Phe1033Ile
NM_005445.3:c.3097T>A , LRG_774t1:c.3097T>A NP_005436.1:p.Phe1033Ile
NM_005445.4:c.3097T>A MANE Select NP_005436.1:p.Phe1033Ile