Canonical Allele Identifier: CA2838018695
Gene: SMC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578686T= , CM000672.2:g.110578686T= GRCh38
NC_000010.10:g.112338444T= , CM000672.1:g.112338444T= GRCh37
NC_000010.9:g.112328434T= NCBI36
NG_012217.1:g.15996T= , LRG_774:g.15996T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.542T=
ENST00000687823.1:n.323T=
ENST00000689932.1:n.2472T=
ENST00000691297.1:n.542T=
ENST00000691527.1:n.1212T=
ENST00000692792.1:n.528T=
ENST00000361804.5:c.409T= MANE Select ENSP00000354720.5:p.Tyr137=
ENST00000361804.4:c.409T= ENSP00000354720.4:p.Tyr137=
ENST00000462899.1:n.555T=
NM_005445.3:c.409T= , LRG_774t1:c.409T= NP_005436.1:p.Tyr137=
NM_005445.4:c.409T= MANE Select NP_005436.1:p.Tyr137=