Canonical Allele Identifier: CA378376348
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112341776A>C (hg19) chr10:g.110582018A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110582018A>C , CM000672.2:g.110582018A>C GRCh38
NC_000010.10:g.112341776A>C , CM000672.1:g.112341776A>C GRCh37
NC_000010.9:g.112331766A>C NCBI36
NG_012217.1:g.19328A>C , LRG_774:g.19328A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.776A>C
ENST00000687823.1:n.557A>C
ENST00000689932.1:n.2706A>C
ENST00000691297.1:n.776A>C
ENST00000691527.1:n.1446A>C
ENST00000692792.1:n.762A>C
ENST00000361804.5:c.643A>C MANE Select ENSP00000354720.5:p.Lys215Gln
ENST00000361804.4:c.643A>C ENSP00000354720.4:p.Lys215Gln
NM_005445.3:c.643A>C , LRG_774t1:c.643A>C NP_005436.1:p.Lys215Gln
NM_005445.4:c.643A>C MANE Select NP_005436.1:p.Lys215Gln
Search 100 bp 5'
Search 100 bp 3'