Canonical Allele Identifier: CA5687659
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs374081444
ExAC: 10:112337161 C / T
gnomAD v2: 10-112337161-C-T
gnomAD v3: 10-110577403-C-T
gnomAD v4: 10-110577403-C-T
MyVariant Identifiers: chr10:g.112337161C>T (hg19) chr10:g.110577403C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110577403C>T , CM000672.2:g.110577403C>T GRCh38
NC_000010.10:g.112337161C>T , CM000672.1:g.112337161C>T GRCh37
NC_000010.9:g.112327151C>T NCBI36
NG_012217.1:g.14713C>T , LRG_774:g.14713C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.332-18C>T
ENST00000687823.1:n.113-18C>T
ENST00000689932.1:n.2262-18C>T
ENST00000691297.1:n.332-18C>T
ENST00000691527.1:n.289-18C>T
ENST00000692792.1:n.318-18C>T
ENST00000361804.5:c.199-18C>T MANE Select ENSP00000354720.5:n.199-18C>T
ENST00000361804.4:c.199-18C>T ENSP00000354720.4:n.199-18C>T
ENST00000462899.1:n.345-18C>T
NM_005445.3:c.199-18C>T , LRG_774t1:c.199-18C>T NP_005436.1:n.199-18C>T
NM_005445.4:c.199-18C>T MANE Select NP_005436.1:n.199-18C>T
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