Canonical Allele Identifier: CA471370367
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112338422T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578664T>C , CM000672.2:g.110578664T>C GRCh38
NC_000010.10:g.112338422T>C , CM000672.1:g.112338422T>C GRCh37
NC_000010.9:g.112328412T>C NCBI36
NG_012217.1:g.15974T>C , LRG_774:g.15974T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.520T>C
ENST00000687823.1:n.301T>C
ENST00000689932.1:n.2450T>C
ENST00000691297.1:n.520T>C
ENST00000691527.1:n.1190T>C
ENST00000692792.1:n.506T>C
ENST00000361804.5:c.387T>C MANE Select ENSP00000354720.5:p.Gly129=
ENST00000361804.4:c.387T>C ENSP00000354720.4:p.Gly129=
ENST00000462899.1:n.533T>C
NM_005445.3:c.387T>C , LRG_774t1:c.387T>C NP_005436.1:p.Gly129=
NM_005445.4:c.387T>C MANE Select NP_005436.1:p.Gly129=
Search 100 bp 5'
Search 100 bp 3'