Canonical Allele Identifier: CA471370363
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112338413A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578655A>G , CM000672.2:g.110578655A>G GRCh38
NC_000010.10:g.112338413A>G , CM000672.1:g.112338413A>G GRCh37
NC_000010.9:g.112328403A>G NCBI36
NG_012217.1:g.15965A>G , LRG_774:g.15965A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.511A>G
ENST00000687823.1:n.292A>G
ENST00000689932.1:n.2441A>G
ENST00000691297.1:n.511A>G
ENST00000691527.1:n.1181A>G
ENST00000692792.1:n.497A>G
ENST00000361804.5:c.378A>G MANE Select ENSP00000354720.5:p.Glu126=
ENST00000361804.4:c.378A>G ENSP00000354720.4:p.Glu126=
ENST00000462899.1:n.524A>G
NM_005445.3:c.378A>G , LRG_774t1:c.378A>G NP_005436.1:p.Glu126=
NM_005445.4:c.378A>G MANE Select NP_005436.1:p.Glu126=
Search 100 bp 5'
Search 100 bp 3'