Canonical Allele Identifier: CA2610887734

Gene: SMC3

Linked Data

• gnomAD v4: 10-110573700-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110573700T>C , CM000672.2:g.110573700T>C	GRCh38
NC_000010.10:g.112333458T>C , CM000672.1:g.112333458T>C	GRCh37
NC_000010.9:g.112323448T>C	NCBI36
NG_012217.1:g.11010T>C , LRG_774:g.11010T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.225-7T>C
ENST00000687823.1:n.45-1636T>C
ENST00000689932.1:n.558T>C
ENST00000691297.1:n.225-7T>C
ENST00000691527.1:n.182-7T>C
ENST00000692792.1:n.211-7T>C
ENST00000361804.5:c.92-7T>C MANE Select	ENSP00000354720.5:n.92-7T>C
ENST00000361804.4:c.92-7T>C	ENSP00000354720.4:n.92-7T>C
ENST00000462899.1:n.238-7T>C
NM_005445.3:c.92-7T>C , LRG_774t1:c.92-7T>C	NP_005436.1:n.92-7T>C
NM_005445.4:c.92-7T>C MANE Select	NP_005436.1:n.92-7T>C