Canonical Allele Identifier: CA213225586
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs537743350
gnomAD v4: 10-110573858-T-C
MyVariant Identifiers: chr10:g.112333616T>C (hg19) chr10:g.110573858T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110573858T>C , CM000672.2:g.110573858T>C GRCh38
NC_000010.10:g.112333616T>C , CM000672.1:g.112333616T>C GRCh37
NC_000010.9:g.112323606T>C NCBI36
NG_012217.1:g.11168T>C , LRG_774:g.11168T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.263+113T>C
ENST00000687823.1:n.45-1478T>C
ENST00000689932.1:n.716T>C
ENST00000691297.1:n.263+113T>C
ENST00000691527.1:n.220+113T>C
ENST00000692792.1:n.249+113T>C
ENST00000361804.5:c.130+113T>C MANE Select ENSP00000354720.5:n.130+113T>C
ENST00000361804.4:c.130+113T>C ENSP00000354720.4:n.130+113T>C
ENST00000462899.1:n.276+113T>C
NM_005445.3:c.130+113T>C , LRG_774t1:c.130+113T>C NP_005436.1:n.130+113T>C
NM_005445.4:c.130+113T>C MANE Select NP_005436.1:n.130+113T>C
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