Canonical Allele Identifier: CA378393598

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112361494T>C (hg19) ; chr10:g.110601736T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110601736T>C , CM000672.2:g.110601736T>C	GRCh38
NC_000010.10:g.112361494T>C , CM000672.1:g.112361494T>C	GRCh37
NC_000010.9:g.112351484T>C	NCBI36
NG_012217.1:g.39046T>C , LRG_774:g.39046T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.4977T>C
ENST00000685743.1:n.2452T>C
ENST00000686057.1:n.1095T>C
ENST00000689321.1:n.1707T>C
ENST00000689986.1:n.533T>C
ENST00000361804.5:c.2744T>C MANE Select	ENSP00000354720.5:p.Ile915Thr
ENST00000361804.4:c.2744T>C	ENSP00000354720.4:p.Ile915Thr
NM_005445.3:c.2744T>C , LRG_774t1:c.2744T>C	NP_005436.1:p.Ile915Thr
NM_005445.4:c.2744T>C MANE Select	NP_005436.1:p.Ile915Thr