Canonical Allele Identifier: CA471370194
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112337250A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110577492A>C , CM000672.2:g.110577492A>C GRCh38
NC_000010.10:g.112337250A>C , CM000672.1:g.112337250A>C GRCh37
NC_000010.9:g.112327240A>C NCBI36
NG_012217.1:g.14802A>C , LRG_774:g.14802A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.403A>C
ENST00000687823.1:n.184A>C
ENST00000689932.1:n.2333A>C
ENST00000691297.1:n.403A>C
ENST00000691527.1:n.360A>C
ENST00000692792.1:n.389A>C
ENST00000361804.5:c.270A>C MANE Select ENSP00000354720.5:p.Pro90=
ENST00000361804.4:c.270A>C ENSP00000354720.4:p.Pro90=
ENST00000462899.1:n.416A>C
NM_005445.3:c.270A>C , LRG_774t1:c.270A>C NP_005436.1:p.Pro90=
NM_005445.4:c.270A>C MANE Select NP_005436.1:p.Pro90=
Search 100 bp 5'
Search 100 bp 3'