Canonical Allele Identifier: CA471505745
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112361429A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601671A>G , CM000672.2:g.110601671A>G GRCh38
NC_000010.10:g.112361429A>G , CM000672.1:g.112361429A>G GRCh37
NC_000010.9:g.112351419A>G NCBI36
NG_012217.1:g.38981A>G , LRG_774:g.38981A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.4912A>G
ENST00000685743.1:n.2387A>G
ENST00000686057.1:n.1030A>G
ENST00000689321.1:n.1642A>G
ENST00000689986.1:n.468A>G
ENST00000361804.5:c.2679A>G MANE Select ENSP00000354720.5:p.Gly893=
ENST00000361804.4:c.2679A>G ENSP00000354720.4:p.Gly893=
NM_005445.3:c.2679A>G , LRG_774t1:c.2679A>G NP_005436.1:p.Gly893=
NM_005445.4:c.2679A>G MANE Select NP_005436.1:p.Gly893=