Canonical Allele Identifier: CA378393649
Gene: SMC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601757T>C , CM000672.2:g.110601757T>C GRCh38
NC_000010.10:g.112361515T>C , CM000672.1:g.112361515T>C GRCh37
NC_000010.9:g.112351505T>C NCBI36
NG_012217.1:g.39067T>C , LRG_774:g.39067T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4998T>C
ENST00000685743.1:n.2473T>C
ENST00000686057.1:n.1116T>C
ENST00000689321.1:n.1728T>C
ENST00000689986.1:n.554T>C
ENST00000361804.5:c.2765T>C MANE Select ENSP00000354720.5:p.Leu922Pro
ENST00000361804.4:c.2765T>C ENSP00000354720.4:p.Leu922Pro
NM_005445.3:c.2765T>C , LRG_774t1:c.2765T>C NP_005436.1:p.Leu922Pro
NM_005445.4:c.2765T>C MANE Select NP_005436.1:p.Leu922Pro