Canonical Allele Identifier: CA471505951
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861390112
MyVariant Identifiers: chr10:g.112361510A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601752A>G , CM000672.2:g.110601752A>G GRCh38
NC_000010.10:g.112361510A>G , CM000672.1:g.112361510A>G GRCh37
NC_000010.9:g.112351500A>G NCBI36
NG_012217.1:g.39062A>G , LRG_774:g.39062A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4993A>G
ENST00000685743.1:n.2468A>G
ENST00000686057.1:n.1111A>G
ENST00000689321.1:n.1723A>G
ENST00000689986.1:n.549A>G
ENST00000361804.5:c.2760A>G MANE Select ENSP00000354720.5:p.Lys920=
ENST00000361804.4:c.2760A>G ENSP00000354720.4:p.Lys920=
NM_005445.3:c.2760A>G , LRG_774t1:c.2760A>G NP_005436.1:p.Lys920=
NM_005445.4:c.2760A>G MANE Select NP_005436.1:p.Lys920=