Canonical Allele Identifier: CA2610883129
Gene: SMC3 HGNC NCBI

Linked Data

gnomAD v4: 10-110577385-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110577385C>A , CM000672.2:g.110577385C>A GRCh38
NC_000010.10:g.112337143C>A , CM000672.1:g.112337143C>A GRCh37
NC_000010.9:g.112327133C>A NCBI36
NG_012217.1:g.14695C>A , LRG_774:g.14695C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.332-36C>A
ENST00000687823.1:n.113-36C>A
ENST00000689932.1:n.2262-36C>A
ENST00000691297.1:n.332-36C>A
ENST00000691527.1:n.289-36C>A
ENST00000692792.1:n.318-36C>A
ENST00000361804.5:c.199-36C>A MANE Select ENSP00000354720.5:n.199-36C>A
ENST00000361804.4:c.199-36C>A ENSP00000354720.4:n.199-36C>A
ENST00000462899.1:n.345-36C>A
NM_005445.3:c.199-36C>A , LRG_774t1:c.199-36C>A NP_005436.1:n.199-36C>A
NM_005445.4:c.199-36C>A MANE Select NP_005436.1:n.199-36C>A
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