Canonical Allele Identifier: CA471505985
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1196080602
gnomAD v2: 10-112361534-G-T
gnomAD v4: 10-110601776-G-T
MyVariant Identifiers: chr10:g.112361534G>T (hg19) chr10:g.110601776G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601776G>T , CM000672.2:g.110601776G>T GRCh38
NC_000010.10:g.112361534G>T , CM000672.1:g.112361534G>T GRCh37
NC_000010.9:g.112351524G>T NCBI36
NG_012217.1:g.39086G>T , LRG_774:g.39086G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5017G>T
ENST00000685743.1:n.2492G>T
ENST00000686057.1:n.1135G>T
ENST00000689321.1:n.1747G>T
ENST00000689986.1:n.573G>T
ENST00000361804.5:c.2784G>T MANE Select ENSP00000354720.5:p.Arg928=
ENST00000361804.4:c.2784G>T ENSP00000354720.4:p.Arg928=
NM_005445.3:c.2784G>T , LRG_774t1:c.2784G>T NP_005436.1:p.Arg928=
NM_005445.4:c.2784G>T MANE Select NP_005436.1:p.Arg928=
Search 100 bp 5'
Search 100 bp 3'