Canonical Allele Identifier: CA471506015
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861395427
MyVariant Identifiers: chr10:g.112361792G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602034G>A , CM000672.2:g.110602034G>A GRCh38
NC_000010.10:g.112361792G>A , CM000672.1:g.112361792G>A GRCh37
NC_000010.9:g.112351782G>A NCBI36
NG_012217.1:g.39344G>A , LRG_774:g.39344G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5194G>A
ENST00000685743.1:n.2669G>A
ENST00000686057.1:n.1312G>A
ENST00000689321.1:n.1924G>A
ENST00000689986.1:n.750G>A
ENST00000361804.5:c.2961G>A MANE Select ENSP00000354720.5:p.Leu987=
ENST00000361804.4:c.2961G>A ENSP00000354720.4:p.Leu987=
NM_005445.3:c.2961G>A , LRG_774t1:c.2961G>A NP_005436.1:p.Leu987=
NM_005445.4:c.2961G>A MANE Select NP_005436.1:p.Leu987=
Search 100 bp 5'
Search 100 bp 3'