Canonical Allele Identifier: CA5688342
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs762809090
ExAC: 10:112361963 TAC / T
gnomAD v2: 10-112361963-TAC-T
gnomAD v3: 10-110602205-TAC-T
gnomAD v4: 10-110602205-TAC-T
COSMIC: COSN25202683
MyVariant Identifiers: chr10:g.112361966_112361967del (hg19) chr10:g.112361964_112361965del (hg19) chr10:g.110602208_110602209del (hg38) chr10:g.110602207_110602208del (hg38) chr10:g.110602206_110602207del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602211_110602212del , CM000672.2:g.110602211_110602212del GRCh38
NC_000010.10:g.112361969_112361970del , CM000672.1:g.112361969_112361970del GRCh37
NC_000010.9:g.112351959_112351960del NCBI36
NG_012217.1:g.39521_39522del , LRG_774:g.39521_39522del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5338+33_5338+34del
ENST00000685743.1:n.2813+33_2813+34del
ENST00000686057.1:n.1456+33_1456+34del
ENST00000689321.1:n.2068+33_2068+34del
ENST00000689986.1:n.894+33_894+34del
ENST00000361804.5:c.3105+33_3105+34del MANE Select ENSP00000354720.5:n.3105+33_3105+34del
ENST00000361804.4:c.3105+33_3105+34del ENSP00000354720.4:n.3105+33_3105+34del
NM_005445.3:c.3105+33_3105+34del , LRG_774t1:c.3105+33_3105+34del NP_005436.1:n.3105+33_3105+34del
NM_005445.4:c.3105+33_3105+34del MANE Select NP_005436.1:n.3105+33_3105+34del
Search 100 bp 5'
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