Canonical Allele Identifier: CA2610888443

Gene: SMC3

Linked Data

• gnomAD v4: 10-110602210-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110602210A>G , CM000672.2:g.110602210A>G	GRCh38
NC_000010.10:g.112361968A>G , CM000672.1:g.112361968A>G	GRCh37
NC_000010.9:g.112351958A>G	NCBI36
NG_012217.1:g.39520A>G , LRG_774:g.39520A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.5338+32A>G
ENST00000685743.1:n.2813+32A>G
ENST00000686057.1:n.1456+32A>G
ENST00000689321.1:n.2068+32A>G
ENST00000689986.1:n.894+32A>G
ENST00000361804.5:c.3105+32A>G MANE Select	ENSP00000354720.5:n.3105+32A>G
ENST00000361804.4:c.3105+32A>G	ENSP00000354720.4:n.3105+32A>G
NM_005445.3:c.3105+32A>G , LRG_774t1:c.3105+32A>G	NP_005436.1:n.3105+32A>G
NM_005445.4:c.3105+32A>G MANE Select	NP_005436.1:n.3105+32A>G