Canonical Allele Identifier: CA2610885192
Gene: SMC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110581840A>C , CM000672.2:g.110581840A>C GRCh38
NC_000010.10:g.112341598A>C , CM000672.1:g.112341598A>C GRCh37
NC_000010.9:g.112331588A>C NCBI36
NG_012217.1:g.19150A>C , LRG_774:g.19150A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.681-83A>C
ENST00000687823.1:n.462-83A>C
ENST00000689932.1:n.2611-83A>C
ENST00000691297.1:n.681-83A>C
ENST00000691527.1:n.1351-83A>C
ENST00000692792.1:n.667-83A>C
ENST00000361804.5:c.548-83A>C MANE Select ENSP00000354720.5:n.548-83A>C
ENST00000361804.4:c.548-83A>C ENSP00000354720.4:n.548-83A>C
ENST00000462899.1:n.694-83A>C
NM_005445.3:c.548-83A>C , LRG_774t1:c.548-83A>C NP_005436.1:n.548-83A>C
NM_005445.4:c.548-83A>C MANE Select NP_005436.1:n.548-83A>C