Canonical Allele Identifier: CA213228779
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs35513050

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578557del , CM000672.2:g.110578557del GRCh38
NC_000010.10:g.112338315del , CM000672.1:g.112338315del GRCh37
NC_000010.9:g.112328305del NCBI36
NG_012217.1:g.15867del , LRG_774:g.15867del

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.484-71del
ENST00000687823.1:n.265-71del
ENST00000689932.1:n.2414-71del
ENST00000691297.1:n.484-71del
ENST00000691527.1:n.1083del
ENST00000692792.1:n.470-71del
ENST00000361804.5:c.351-71del MANE Select ENSP00000354720.5:n.351-71del
ENST00000361804.4:c.351-71del ENSP00000354720.4:n.351-71del
ENST00000462899.1:n.497-71del
NM_005445.3:c.351-71del , LRG_774t1:c.351-71del NP_005436.1:n.351-71del
NM_005445.4:c.351-71del MANE Select NP_005436.1:n.351-71del