Canonical Allele Identifier: CA471506009
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112361786G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602028G>A , CM000672.2:g.110602028G>A GRCh38
NC_000010.10:g.112361786G>A , CM000672.1:g.112361786G>A GRCh37
NC_000010.9:g.112351776G>A NCBI36
NG_012217.1:g.39338G>A , LRG_774:g.39338G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5188G>A
ENST00000685743.1:n.2663G>A
ENST00000686057.1:n.1306G>A
ENST00000689321.1:n.1918G>A
ENST00000689986.1:n.744G>A
ENST00000361804.5:c.2955G>A MANE Select ENSP00000354720.5:p.Lys985=
ENST00000361804.4:c.2955G>A ENSP00000354720.4:p.Lys985=
NM_005445.3:c.2955G>A , LRG_774t1:c.2955G>A NP_005436.1:p.Lys985=
NM_005445.4:c.2955G>A MANE Select NP_005436.1:p.Lys985=
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