Canonical Allele Identifier: CA471370188

Gene: SMC3

Linked Data

• MyVariant Identifiers: chr10:g.112337241C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110577483C>T , CM000672.2:g.110577483C>T	GRCh38
NC_000010.10:g.112337241C>T , CM000672.1:g.112337241C>T	GRCh37
NC_000010.9:g.112327231C>T	NCBI36
NG_012217.1:g.14793C>T , LRG_774:g.14793C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.394C>T
ENST00000687823.1:n.175C>T
ENST00000689932.1:n.2324C>T
ENST00000691297.1:n.394C>T
ENST00000691527.1:n.351C>T
ENST00000692792.1:n.380C>T
ENST00000361804.5:c.261C>T MANE Select	ENSP00000354720.5:p.Asn87=
ENST00000361804.4:c.261C>T	ENSP00000354720.4:p.Asn87=
ENST00000462899.1:n.407C>T
NM_005445.3:c.261C>T , LRG_774t1:c.261C>T	NP_005436.1:p.Asn87=
NM_005445.4:c.261C>T MANE Select	NP_005436.1:p.Asn87=