Canonical Allele Identifier: CA471370357

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112338398G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110578640G>C , CM000672.2:g.110578640G>C	GRCh38
NC_000010.10:g.112338398G>C , CM000672.1:g.112338398G>C	GRCh37
NC_000010.9:g.112328388G>C	NCBI36
NG_012217.1:g.15950G>C , LRG_774:g.15950G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.496G>C
ENST00000687823.1:n.277G>C
ENST00000689932.1:n.2426G>C
ENST00000691297.1:n.496G>C
ENST00000691527.1:n.1166G>C
ENST00000692792.1:n.482G>C
ENST00000361804.5:c.363G>C MANE Select	ENSP00000354720.5:p.Val121=
ENST00000361804.4:c.363G>C	ENSP00000354720.4:p.Val121=
ENST00000462899.1:n.509G>C
NM_005445.3:c.363G>C , LRG_774t1:c.363G>C	NP_005436.1:p.Val121=
NM_005445.4:c.363G>C MANE Select	NP_005436.1:p.Val121=