Canonical Allele Identifier: CA471506085
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112361891A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602133A>C , CM000672.2:g.110602133A>C GRCh38
NC_000010.10:g.112361891A>C , CM000672.1:g.112361891A>C GRCh37
NC_000010.9:g.112351881A>C NCBI36
NG_012217.1:g.39443A>C , LRG_774:g.39443A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5293A>C
ENST00000685743.1:n.2768A>C
ENST00000686057.1:n.1411A>C
ENST00000689321.1:n.2023A>C
ENST00000689986.1:n.849A>C
ENST00000361804.5:c.3060A>C MANE Select ENSP00000354720.5:p.Val1020=
ENST00000361804.4:c.3060A>C ENSP00000354720.4:p.Val1020=
NM_005445.3:c.3060A>C , LRG_774t1:c.3060A>C NP_005436.1:p.Val1020=
NM_005445.4:c.3060A>C MANE Select NP_005436.1:p.Val1020=
Search 100 bp 5'
Search 100 bp 3'