Canonical Allele Identifier: CA378371917

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112337236G>T (hg19) ; chr10:g.110577478G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110577478G>T , CM000672.2:g.110577478G>T	GRCh38
NC_000010.10:g.112337236G>T , CM000672.1:g.112337236G>T	GRCh37
NC_000010.9:g.112327226G>T	NCBI36
NG_012217.1:g.14788G>T , LRG_774:g.14788G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684988.1:n.389G>T
ENST00000687823.1:n.170G>T
ENST00000689932.1:n.2319G>T
ENST00000691297.1:n.389G>T
ENST00000691527.1:n.346G>T
ENST00000692792.1:n.375G>T
ENST00000361804.5:c.256G>T MANE Select	ENSP00000354720.5:p.Asp86Tyr
ENST00000361804.4:c.256G>T	ENSP00000354720.4:p.Asp86Tyr
ENST00000462899.1:n.402G>T
NM_005445.3:c.256G>T , LRG_774t1:c.256G>T	NP_005436.1:p.Asp86Tyr
NM_005445.4:c.256G>T MANE Select	NP_005436.1:p.Asp86Tyr