Canonical Allele Identifier: CA378369853

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112335111A>C (hg19) ; chr10:g.110575353A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110575353A>C , CM000672.2:g.110575353A>C	GRCh38
NC_000010.10:g.112335111A>C , CM000672.1:g.112335111A>C	GRCh37
NC_000010.9:g.112325101A>C	NCBI36
NG_012217.1:g.12663A>C , LRG_774:g.12663A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.281A>C
ENST00000687823.1:n.62A>C
ENST00000689932.1:n.2211A>C
ENST00000691297.1:n.281A>C
ENST00000691527.1:n.238A>C
ENST00000692792.1:n.267A>C
ENST00000361804.5:c.148A>C MANE Select	ENSP00000354720.5:p.Ser50Arg
ENST00000361804.4:c.148A>C	ENSP00000354720.4:p.Ser50Arg
ENST00000462899.1:n.294A>C
NM_005445.3:c.148A>C , LRG_774t1:c.148A>C	NP_005436.1:p.Ser50Arg
NM_005445.4:c.148A>C MANE Select	NP_005436.1:p.Ser50Arg