Canonical Allele Identifier: CA378394367
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112361890T>G (hg19) chr10:g.110602132T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602132T>G , CM000672.2:g.110602132T>G GRCh38
NC_000010.10:g.112361890T>G , CM000672.1:g.112361890T>G GRCh37
NC_000010.9:g.112351880T>G NCBI36
NG_012217.1:g.39442T>G , LRG_774:g.39442T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5292T>G
ENST00000685743.1:n.2767T>G
ENST00000686057.1:n.1410T>G
ENST00000689321.1:n.2022T>G
ENST00000689986.1:n.848T>G
ENST00000361804.5:c.3059T>G MANE Select ENSP00000354720.5:p.Val1020Gly
ENST00000361804.4:c.3059T>G ENSP00000354720.4:p.Val1020Gly
NM_005445.3:c.3059T>G , LRG_774t1:c.3059T>G NP_005436.1:p.Val1020Gly
NM_005445.4:c.3059T>G MANE Select NP_005436.1:p.Val1020Gly
Search 100 bp 5'
Search 100 bp 3'