Canonical Allele Identifier: CA378393387
Gene: SMC3 HGNC NCBI

Linked Data

gnomAD v4: 10-110601649-C-A
MyVariant Identifiers: chr10:g.112361407C>A (hg19) chr10:g.110601649C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601649C>A , CM000672.2:g.110601649C>A GRCh38
NC_000010.10:g.112361407C>A , CM000672.1:g.112361407C>A GRCh37
NC_000010.9:g.112351397C>A NCBI36
NG_012217.1:g.38959C>A , LRG_774:g.38959C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4890C>A
ENST00000685743.1:n.2365C>A
ENST00000686057.1:n.1008C>A
ENST00000689321.1:n.1620C>A
ENST00000689986.1:n.446C>A
ENST00000361804.5:c.2657C>A MANE Select ENSP00000354720.5:p.Ser886Tyr
ENST00000361804.4:c.2657C>A ENSP00000354720.4:p.Ser886Tyr
NM_005445.3:c.2657C>A , LRG_774t1:c.2657C>A NP_005436.1:p.Ser886Tyr
NM_005445.4:c.2657C>A MANE Select NP_005436.1:p.Ser886Tyr
Search 100 bp 5'
Search 100 bp 3'