Canonical Allele Identifier: CA2610883872

Gene: SMC3

Linked Data

• gnomAD v4: 10-110578586-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110578586T>C , CM000672.2:g.110578586T>C	GRCh38
NC_000010.10:g.112338344T>C , CM000672.1:g.112338344T>C	GRCh37
NC_000010.9:g.112328334T>C	NCBI36
NG_012217.1:g.15896T>C , LRG_774:g.15896T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684988.1:n.484-42T>C
ENST00000687823.1:n.265-42T>C
ENST00000689932.1:n.2414-42T>C
ENST00000691297.1:n.484-42T>C
ENST00000691527.1:n.1112T>C
ENST00000692792.1:n.470-42T>C
ENST00000361804.5:c.351-42T>C MANE Select	ENSP00000354720.5:n.351-42T>C
ENST00000361804.4:c.351-42T>C	ENSP00000354720.4:n.351-42T>C
ENST00000462899.1:n.497-42T>C
NM_005445.3:c.351-42T>C , LRG_774t1:c.351-42T>C	NP_005436.1:n.351-42T>C
NM_005445.4:c.351-42T>C MANE Select	NP_005436.1:n.351-42T>C