Canonical Allele Identifier: CA5688331
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs775544781
ExAC: 10:112361941 G / T
gnomAD v2: 10-112361941-G-T
gnomAD v4: 10-110602183-G-T
MyVariant Identifiers: chr10:g.112361941G>T (hg19) chr10:g.110602183G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110602183G>T , CM000672.2:g.110602183G>T GRCh38
NC_000010.10:g.112361941G>T , CM000672.1:g.112361941G>T GRCh37
NC_000010.9:g.112351931G>T NCBI36
NG_012217.1:g.39493G>T , LRG_774:g.39493G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.5338+5G>T
ENST00000685743.1:n.2813+5G>T
ENST00000686057.1:n.1456+5G>T
ENST00000689321.1:n.2068+5G>T
ENST00000689986.1:n.894+5G>T
ENST00000361804.5:c.3105+5G>T MANE Select ENSP00000354720.5:n.3105+5G>T
ENST00000361804.4:c.3105+5G>T ENSP00000354720.4:n.3105+5G>T
NM_005445.3:c.3105+5G>T , LRG_774t1:c.3105+5G>T NP_005436.1:n.3105+5G>T
NM_005445.4:c.3105+5G>T MANE Select NP_005436.1:n.3105+5G>T
Search 100 bp 5'
Search 100 bp 3'