Canonical Allele Identifier: CA2610883138

Gene: SMC3

Linked Data

• gnomAD v4: 10-110577398-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110577398T>C , CM000672.2:g.110577398T>C	GRCh38
NC_000010.10:g.112337156T>C , CM000672.1:g.112337156T>C	GRCh37
NC_000010.9:g.112327146T>C	NCBI36
NG_012217.1:g.14708T>C , LRG_774:g.14708T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.332-23T>C
ENST00000687823.1:n.113-23T>C
ENST00000689932.1:n.2262-23T>C
ENST00000691297.1:n.332-23T>C
ENST00000691527.1:n.289-23T>C
ENST00000692792.1:n.318-23T>C
ENST00000361804.5:c.199-23T>C MANE Select	ENSP00000354720.5:n.199-23T>C
ENST00000361804.4:c.199-23T>C	ENSP00000354720.4:n.199-23T>C
ENST00000462899.1:n.345-23T>C
NM_005445.3:c.199-23T>C , LRG_774t1:c.199-23T>C	NP_005436.1:n.199-23T>C
NM_005445.4:c.199-23T>C MANE Select	NP_005436.1:n.199-23T>C