Canonical Allele Identifier: CA2610887772

Gene: SMC3

Linked Data

• gnomAD v4: 10-110601607-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110601607A>T , CM000672.2:g.110601607A>T	GRCh38
NC_000010.10:g.112361365A>T , CM000672.1:g.112361365A>T	GRCh37
NC_000010.9:g.112351355A>T	NCBI36
NG_012217.1:g.38917A>T , LRG_774:g.38917A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.4878-30A>T
ENST00000685743.1:n.2323A>T
ENST00000686057.1:n.996-30A>T
ENST00000689321.1:n.1608-30A>T
ENST00000689986.1:n.434-30A>T
ENST00000361804.5:c.2645-30A>T MANE Select	ENSP00000354720.5:n.2645-30A>T
ENST00000361804.4:c.2645-30A>T	ENSP00000354720.4:n.2645-30A>T
NM_005445.3:c.2645-30A>T , LRG_774t1:c.2645-30A>T	NP_005436.1:n.2645-30A>T
NM_005445.4:c.2645-30A>T MANE Select	NP_005436.1:n.2645-30A>T