Canonical Allele Identifier: CA378393616
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861390022

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601744G>A , CM000672.2:g.110601744G>A GRCh38
NC_000010.10:g.112361502G>A , CM000672.1:g.112361502G>A GRCh37
NC_000010.9:g.112351492G>A NCBI36
NG_012217.1:g.39054G>A , LRG_774:g.39054G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4985G>A
ENST00000685743.1:n.2460G>A
ENST00000686057.1:n.1103G>A
ENST00000689321.1:n.1715G>A
ENST00000689986.1:n.541G>A
ENST00000361804.5:c.2752G>A MANE Select ENSP00000354720.5:p.Asp918Asn
ENST00000361804.4:c.2752G>A ENSP00000354720.4:p.Asp918Asn
NM_005445.3:c.2752G>A , LRG_774t1:c.2752G>A NP_005436.1:p.Asp918Asn
NM_005445.4:c.2752G>A MANE Select NP_005436.1:p.Asp918Asn