Canonical Allele Identifier: CA213249135
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1007259461
gnomAD v3: 10-110601653-T-C
gnomAD v4: 10-110601653-T-C
MyVariant Identifiers: chr10:g.112361411T>C (hg19) chr10:g.110601653T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601653T>C , CM000672.2:g.110601653T>C GRCh38
NC_000010.10:g.112361411T>C , CM000672.1:g.112361411T>C GRCh37
NC_000010.9:g.112351401T>C NCBI36
NG_012217.1:g.38963T>C , LRG_774:g.38963T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4894T>C
ENST00000685743.1:n.2369T>C
ENST00000686057.1:n.1012T>C
ENST00000689321.1:n.1624T>C
ENST00000689986.1:n.450T>C
ENST00000361804.5:c.2661T>C MANE Select ENSP00000354720.5:p.Ile887=
ENST00000361804.4:c.2661T>C ENSP00000354720.4:p.Ile887=
NM_005445.3:c.2661T>C , LRG_774t1:c.2661T>C NP_005436.1:p.Ile887=
NM_005445.4:c.2661T>C MANE Select NP_005436.1:p.Ile887=
Search 100 bp 5'
Search 100 bp 3'