Canonical Allele Identifier: CA378393394

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112361410T>C (hg19) ; chr10:g.110601652T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110601652T>C , CM000672.2:g.110601652T>C	GRCh38
NC_000010.10:g.112361410T>C , CM000672.1:g.112361410T>C	GRCh37
NC_000010.9:g.112351400T>C	NCBI36
NG_012217.1:g.38962T>C , LRG_774:g.38962T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.4893T>C
ENST00000685743.1:n.2368T>C
ENST00000686057.1:n.1011T>C
ENST00000689321.1:n.1623T>C
ENST00000689986.1:n.449T>C
ENST00000361804.5:c.2660T>C MANE Select	ENSP00000354720.5:p.Ile887Thr
ENST00000361804.4:c.2660T>C	ENSP00000354720.4:p.Ile887Thr
NM_005445.3:c.2660T>C , LRG_774t1:c.2660T>C	NP_005436.1:p.Ile887Thr
NM_005445.4:c.2660T>C MANE Select	NP_005436.1:p.Ile887Thr