Canonical Allele Identifier: CA378373849

Gene: SMC3

Linked Data

• gnomAD v4: 10-110578660-C-T
• MyVariant Identifiers: chr10:g.112338418C>T (hg19) ; chr10:g.110578660C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110578660C>T , CM000672.2:g.110578660C>T	GRCh38
NC_000010.10:g.112338418C>T , CM000672.1:g.112338418C>T	GRCh37
NC_000010.9:g.112328408C>T	NCBI36
NG_012217.1:g.15970C>T , LRG_774:g.15970C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684988.1:n.516C>T
ENST00000687823.1:n.297C>T
ENST00000689932.1:n.2446C>T
ENST00000691297.1:n.516C>T
ENST00000691527.1:n.1186C>T
ENST00000692792.1:n.502C>T
ENST00000361804.5:c.383C>T MANE Select	ENSP00000354720.5:p.Ala128Val
ENST00000361804.4:c.383C>T	ENSP00000354720.4:p.Ala128Val
ENST00000462899.1:n.529C>T
NM_005445.3:c.383C>T , LRG_774t1:c.383C>T	NP_005436.1:p.Ala128Val
NM_005445.4:c.383C>T MANE Select	NP_005436.1:p.Ala128Val