Canonical Allele Identifier: CA378393380
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861388930

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601646A>G , CM000672.2:g.110601646A>G GRCh38
NC_000010.10:g.112361404A>G , CM000672.1:g.112361404A>G GRCh37
NC_000010.9:g.112351394A>G NCBI36
NG_012217.1:g.38956A>G , LRG_774:g.38956A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4887A>G
ENST00000685743.1:n.2362A>G
ENST00000686057.1:n.1005A>G
ENST00000689321.1:n.1617A>G
ENST00000689986.1:n.443A>G
ENST00000361804.5:c.2654A>G MANE Select ENSP00000354720.5:p.Asn885Ser
ENST00000361804.4:c.2654A>G ENSP00000354720.4:p.Asn885Ser
NM_005445.3:c.2654A>G , LRG_774t1:c.2654A>G NP_005436.1:p.Asn885Ser
NM_005445.4:c.2654A>G MANE Select NP_005436.1:p.Asn885Ser