Canonical Allele Identifier: CA2722630667

Gene: SMC3

Linked Data

• dbSNP Id: rs185674152

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110573439C>G , CM000672.2:g.110573439C>G	GRCh38
NC_000010.10:g.112333197C>G , CM000672.1:g.112333197C>G	GRCh37
NC_000010.9:g.112323187C>G	NCBI36
NG_012217.1:g.10749C>G , LRG_774:g.10749C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.225-268C>G
ENST00000687823.1:n.45-1897C>G
ENST00000689932.1:n.297C>G
ENST00000691297.1:n.225-268C>G
ENST00000691527.1:n.182-268C>G
ENST00000692792.1:n.211-268C>G
ENST00000361804.5:c.92-268C>G MANE Select	ENSP00000354720.5:n.92-268C>G
ENST00000361804.4:c.92-268C>G	ENSP00000354720.4:n.92-268C>G
ENST00000462899.1:n.238-268C>G
NM_005445.3:c.92-268C>G , LRG_774t1:c.92-268C>G	NP_005436.1:n.92-268C>G
NM_005445.4:c.92-268C>G MANE Select	NP_005436.1:n.92-268C>G