Canonical Allele Identifier: CA2610887766
Gene: SMC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601600A>G , CM000672.2:g.110601600A>G GRCh38
NC_000010.10:g.112361358A>G , CM000672.1:g.112361358A>G GRCh37
NC_000010.9:g.112351348A>G NCBI36
NG_012217.1:g.38910A>G , LRG_774:g.38910A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4878-37A>G
ENST00000685743.1:n.2316A>G
ENST00000686057.1:n.996-37A>G
ENST00000689321.1:n.1608-37A>G
ENST00000689986.1:n.434-37A>G
ENST00000361804.5:c.2645-37A>G MANE Select ENSP00000354720.5:n.2645-37A>G
ENST00000361804.4:c.2645-37A>G ENSP00000354720.4:n.2645-37A>G
NM_005445.3:c.2645-37A>G , LRG_774t1:c.2645-37A>G NP_005436.1:n.2645-37A>G
NM_005445.4:c.2645-37A>G MANE Select NP_005436.1:n.2645-37A>G