Canonical Allele Identifier: CA659783025
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1406262824
MyVariant Identifiers: chr10:g.112338321C>G (hg19) chr10:g.110578563C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578563C>G , CM000672.2:g.110578563C>G GRCh38
NC_000010.10:g.112338321C>G , CM000672.1:g.112338321C>G GRCh37
NC_000010.9:g.112328311C>G NCBI36
NG_012217.1:g.15873C>G , LRG_774:g.15873C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.484-65C>G
ENST00000687823.1:n.265-65C>G
ENST00000689932.1:n.2414-65C>G
ENST00000691297.1:n.484-65C>G
ENST00000691527.1:n.1089C>G
ENST00000692792.1:n.470-65C>G
ENST00000361804.5:c.351-65C>G MANE Select ENSP00000354720.5:n.351-65C>G
ENST00000361804.4:c.351-65C>G ENSP00000354720.4:n.351-65C>G
ENST00000462899.1:n.497-65C>G
NM_005445.3:c.351-65C>G , LRG_774t1:c.351-65C>G NP_005436.1:n.351-65C>G
NM_005445.4:c.351-65C>G MANE Select NP_005436.1:n.351-65C>G
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