Canonical Allele Identifier: CA378373845

Gene: SMC3

Linked Data

• gnomAD v4: 10-110578659-G-T
• MyVariant Identifiers: chr10:g.112338417G>T (hg19) ; chr10:g.110578659G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110578659G>T , CM000672.2:g.110578659G>T	GRCh38
NC_000010.10:g.112338417G>T , CM000672.1:g.112338417G>T	GRCh37
NC_000010.9:g.112328407G>T	NCBI36
NG_012217.1:g.15969G>T , LRG_774:g.15969G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684988.1:n.515G>T
ENST00000687823.1:n.296G>T
ENST00000689932.1:n.2445G>T
ENST00000691297.1:n.515G>T
ENST00000691527.1:n.1185G>T
ENST00000692792.1:n.501G>T
ENST00000361804.5:c.382G>T MANE Select	ENSP00000354720.5:p.Ala128Ser
ENST00000361804.4:c.382G>T	ENSP00000354720.4:p.Ala128Ser
ENST00000462899.1:n.528G>T
NM_005445.3:c.382G>T , LRG_774t1:c.382G>T	NP_005436.1:p.Ala128Ser
NM_005445.4:c.382G>T MANE Select	NP_005436.1:p.Ala128Ser