Canonical Allele Identifier: CA5688274
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs763199067

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601657A>G , CM000672.2:g.110601657A>G GRCh38
NC_000010.10:g.112361415A>G , CM000672.1:g.112361415A>G GRCh37
NC_000010.9:g.112351405A>G NCBI36
NG_012217.1:g.38967A>G , LRG_774:g.38967A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4898A>G
ENST00000685743.1:n.2373A>G
ENST00000686057.1:n.1016A>G
ENST00000689321.1:n.1628A>G
ENST00000689986.1:n.454A>G
ENST00000361804.5:c.2665A>G MANE Select ENSP00000354720.5:p.Lys889Glu
ENST00000361804.4:c.2665A>G ENSP00000354720.4:p.Lys889Glu
NM_005445.3:c.2665A>G , LRG_774t1:c.2665A>G NP_005436.1:p.Lys889Glu
NM_005445.4:c.2665A>G MANE Select NP_005436.1:p.Lys889Glu