Canonical Allele Identifier: CA5687720
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs766523518
ExAC: 10:112338358 G / A
gnomAD v2: 10-112338358-G-A
gnomAD v3: 10-110578600-G-A
gnomAD v4: 10-110578600-G-A
MyVariant Identifiers: chr10:g.112338358G>A (hg19) chr10:g.110578600G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578600G>A , CM000672.2:g.110578600G>A GRCh38
NC_000010.10:g.112338358G>A , CM000672.1:g.112338358G>A GRCh37
NC_000010.9:g.112328348G>A NCBI36
NG_012217.1:g.15910G>A , LRG_774:g.15910G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.484-28G>A
ENST00000687823.1:n.265-28G>A
ENST00000689932.1:n.2414-28G>A
ENST00000691297.1:n.484-28G>A
ENST00000691527.1:n.1126G>A
ENST00000692792.1:n.470-28G>A
ENST00000361804.5:c.351-28G>A MANE Select ENSP00000354720.5:n.351-28G>A
ENST00000361804.4:c.351-28G>A ENSP00000354720.4:n.351-28G>A
ENST00000462899.1:n.497-28G>A
NM_005445.3:c.351-28G>A , LRG_774t1:c.351-28G>A NP_005436.1:n.351-28G>A
NM_005445.4:c.351-28G>A MANE Select NP_005436.1:n.351-28G>A
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