Canonical Allele Identifier: CA2610883142
Gene: SMC3 HGNC NCBI

Linked Data

gnomAD v4: 10-110577402-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110577402T>C , CM000672.2:g.110577402T>C GRCh38
NC_000010.10:g.112337160T>C , CM000672.1:g.112337160T>C GRCh37
NC_000010.9:g.112327150T>C NCBI36
NG_012217.1:g.14712T>C , LRG_774:g.14712T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.332-19T>C
ENST00000687823.1:n.113-19T>C
ENST00000689932.1:n.2262-19T>C
ENST00000691297.1:n.332-19T>C
ENST00000691527.1:n.289-19T>C
ENST00000692792.1:n.318-19T>C
ENST00000361804.5:c.199-19T>C MANE Select ENSP00000354720.5:n.199-19T>C
ENST00000361804.4:c.199-19T>C ENSP00000354720.4:n.199-19T>C
ENST00000462899.1:n.345-19T>C
NM_005445.3:c.199-19T>C , LRG_774t1:c.199-19T>C NP_005436.1:n.199-19T>C
NM_005445.4:c.199-19T>C MANE Select NP_005436.1:n.199-19T>C
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