Canonical Allele Identifier: CA2610887676
Gene: SMC3 HGNC NCBI

Linked Data

gnomAD v4: 10-110573684-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110573684T>A , CM000672.2:g.110573684T>A GRCh38
NC_000010.10:g.112333442T>A , CM000672.1:g.112333442T>A GRCh37
NC_000010.9:g.112323432T>A NCBI36
NG_012217.1:g.10994T>A , LRG_774:g.10994T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.225-23T>A
ENST00000687823.1:n.45-1652T>A
ENST00000689932.1:n.542T>A
ENST00000691297.1:n.225-23T>A
ENST00000691527.1:n.182-23T>A
ENST00000692792.1:n.211-23T>A
ENST00000361804.5:c.92-23T>A MANE Select ENSP00000354720.5:n.92-23T>A
ENST00000361804.4:c.92-23T>A ENSP00000354720.4:n.92-23T>A
ENST00000462899.1:n.238-23T>A
NM_005445.3:c.92-23T>A , LRG_774t1:c.92-23T>A NP_005436.1:n.92-23T>A
NM_005445.4:c.92-23T>A MANE Select NP_005436.1:n.92-23T>A
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