Canonical Allele Identifier: CA10634539
Gene: SMC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 298762
ClinVar RCV Id: RCV000272720
dbSNP Id: rs886046692
gnomAD v3: 10-110567752-T-A
gnomAD v4: 10-110567752-T-A
MyVariant Identifiers: chr10:g.112327510T>A (hg19) chr10:g.110567752T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110567752T>A , CM000672.2:g.110567752T>A GRCh38
NC_000010.10:g.112327510T>A , CM000672.1:g.112327510T>A GRCh37
NC_000010.9:g.112317500T>A NCBI36
NG_012217.1:g.5062T>A , LRG_774:g.5062T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.69T>A
ENST00000691297.1:n.69T>A
ENST00000691527.1:n.26T>A
ENST00000361804.5:c.-65T>A MANE Select ENSP00000354720.5:n.-65T>A
ENST00000361804.4:c.-65T>A ENSP00000354720.4:n.-65T>A
NM_005445.3:c.-65T>A , LRG_774t1:c.-65T>A NP_005436.1:n.-65T>A
NM_005445.4:c.-65T>A MANE Select NP_005436.1:n.-65T>A
Search 100 bp 5'
Search 100 bp 3'