Canonical Allele Identifier: CA378393485
Gene: SMC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601692T>A , CM000672.2:g.110601692T>A GRCh38
NC_000010.10:g.112361450T>A , CM000672.1:g.112361450T>A GRCh37
NC_000010.9:g.112351440T>A NCBI36
NG_012217.1:g.39002T>A , LRG_774:g.39002T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.4933T>A
ENST00000685743.1:n.2408T>A
ENST00000686057.1:n.1051T>A
ENST00000689321.1:n.1663T>A
ENST00000689986.1:n.489T>A
ENST00000361804.5:c.2700T>A MANE Select ENSP00000354720.5:p.Ser900Arg
ENST00000361804.4:c.2700T>A ENSP00000354720.4:p.Ser900Arg
NM_005445.3:c.2700T>A , LRG_774t1:c.2700T>A NP_005436.1:p.Ser900Arg
NM_005445.4:c.2700T>A MANE Select NP_005436.1:p.Ser900Arg