Canonical Allele Identifier: CA2610883127
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1860968278
gnomAD v4: 10-110577384-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110577384A>G , CM000672.2:g.110577384A>G GRCh38
NC_000010.10:g.112337142A>G , CM000672.1:g.112337142A>G GRCh37
NC_000010.9:g.112327132A>G NCBI36
NG_012217.1:g.14694A>G , LRG_774:g.14694A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.332-37A>G
ENST00000687823.1:n.113-37A>G
ENST00000689932.1:n.2262-37A>G
ENST00000691297.1:n.332-37A>G
ENST00000691527.1:n.289-37A>G
ENST00000692792.1:n.318-37A>G
ENST00000361804.5:c.199-37A>G MANE Select ENSP00000354720.5:n.199-37A>G
ENST00000361804.4:c.199-37A>G ENSP00000354720.4:n.199-37A>G
ENST00000462899.1:n.345-37A>G
NM_005445.3:c.199-37A>G , LRG_774t1:c.199-37A>G NP_005436.1:n.199-37A>G
NM_005445.4:c.199-37A>G MANE Select NP_005436.1:n.199-37A>G
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