Canonical Allele Identifier: CA378394473
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861397387
MyVariant Identifiers: chr10:g.112361937G>A (hg19) chr10:g.110602179G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602179G>A , CM000672.2:g.110602179G>A GRCh38
NC_000010.10:g.112361937G>A , CM000672.1:g.112361937G>A GRCh37
NC_000010.9:g.112351927G>A NCBI36
NG_012217.1:g.39489G>A , LRG_774:g.39489G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5338+1G>A
ENST00000685743.1:n.2813+1G>A
ENST00000686057.1:n.1456+1G>A
ENST00000689321.1:n.2068+1G>A
ENST00000689986.1:n.894+1G>A
ENST00000361804.5:c.3105+1G>A MANE Select ENSP00000354720.5:n.3105+1G>A
ENST00000361804.4:c.3105+1G>A ENSP00000354720.4:n.3105+1G>A
NM_005445.3:c.3105+1G>A , LRG_774t1:c.3105+1G>A NP_005436.1:n.3105+1G>A
NM_005445.4:c.3105+1G>A MANE Select NP_005436.1:n.3105+1G>A
Search 100 bp 5'
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