Canonical Allele Identifier: CA471370792

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112341796A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110582038A>C , CM000672.2:g.110582038A>C	GRCh38
NC_000010.10:g.112341796A>C , CM000672.1:g.112341796A>C	GRCh37
NC_000010.9:g.112331786A>C	NCBI36
NG_012217.1:g.19348A>C , LRG_774:g.19348A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.796A>C
ENST00000687823.1:n.577A>C
ENST00000689932.1:n.2726A>C
ENST00000691297.1:n.796A>C
ENST00000691527.1:n.1466A>C
ENST00000692792.1:n.782A>C
ENST00000361804.5:c.663A>C MANE Select	ENSP00000354720.5:p.Arg221=
ENST00000361804.4:c.663A>C	ENSP00000354720.4:p.Arg221=
NM_005445.3:c.663A>C , LRG_774t1:c.663A>C	NP_005436.1:p.Arg221=
NM_005445.4:c.663A>C MANE Select	NP_005436.1:p.Arg221=