Canonical Allele Identifier: CA471370364
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112338419T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110578661T>A , CM000672.2:g.110578661T>A GRCh38
NC_000010.10:g.112338419T>A , CM000672.1:g.112338419T>A GRCh37
NC_000010.9:g.112328409T>A NCBI36
NG_012217.1:g.15971T>A , LRG_774:g.15971T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.517T>A
ENST00000687823.1:n.298T>A
ENST00000689932.1:n.2447T>A
ENST00000691297.1:n.517T>A
ENST00000691527.1:n.1187T>A
ENST00000692792.1:n.503T>A
ENST00000361804.5:c.384T>A MANE Select ENSP00000354720.5:p.Ala128=
ENST00000361804.4:c.384T>A ENSP00000354720.4:p.Ala128=
ENST00000462899.1:n.530T>A
NM_005445.3:c.384T>A , LRG_774t1:c.384T>A NP_005436.1:p.Ala128=
NM_005445.4:c.384T>A MANE Select NP_005436.1:p.Ala128=