Canonical Allele Identifier: CA2722791201
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1860902784
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110573492T>C , CM000672.2:g.110573492T>C GRCh38
NC_000010.10:g.112333250T>C , CM000672.1:g.112333250T>C GRCh37
NC_000010.9:g.112323240T>C NCBI36
NG_012217.1:g.10802T>C , LRG_774:g.10802T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.225-215T>C
ENST00000687823.1:n.45-1844T>C
ENST00000689932.1:n.350T>C
ENST00000691297.1:n.225-215T>C
ENST00000691527.1:n.182-215T>C
ENST00000692792.1:n.211-215T>C
ENST00000361804.5:c.92-215T>C MANE Select ENSP00000354720.5:n.92-215T>C
ENST00000361804.4:c.92-215T>C ENSP00000354720.4:n.92-215T>C
ENST00000462899.1:n.238-215T>C
NM_005445.3:c.92-215T>C , LRG_774t1:c.92-215T>C NP_005436.1:n.92-215T>C
NM_005445.4:c.92-215T>C MANE Select NP_005436.1:n.92-215T>C
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