Canonical Allele Identifier: CA2610887749
Gene: SMC3 HGNC NCBI

Linked Data

gnomAD v4: 10-110601576-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601576C>A , CM000672.2:g.110601576C>A GRCh38
NC_000010.10:g.112361334C>A , CM000672.1:g.112361334C>A GRCh37
NC_000010.9:g.112351324C>A NCBI36
NG_012217.1:g.38886C>A , LRG_774:g.38886C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4878-61C>A
ENST00000685743.1:n.2292C>A
ENST00000686057.1:n.996-61C>A
ENST00000689321.1:n.1608-61C>A
ENST00000689986.1:n.434-61C>A
ENST00000361804.5:c.2645-61C>A MANE Select ENSP00000354720.5:n.2645-61C>A
ENST00000361804.4:c.2645-61C>A ENSP00000354720.4:n.2645-61C>A
NM_005445.3:c.2645-61C>A , LRG_774t1:c.2645-61C>A NP_005436.1:n.2645-61C>A
NM_005445.4:c.2645-61C>A MANE Select NP_005436.1:n.2645-61C>A
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