Canonical Allele Identifier: CA471370752
Gene: SMC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112341775G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110582017G>A , CM000672.2:g.110582017G>A GRCh38
NC_000010.10:g.112341775G>A , CM000672.1:g.112341775G>A GRCh37
NC_000010.9:g.112331765G>A NCBI36
NG_012217.1:g.19327G>A , LRG_774:g.19327G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684988.1:n.775G>A
ENST00000687823.1:n.556G>A
ENST00000689932.1:n.2705G>A
ENST00000691297.1:n.775G>A
ENST00000691527.1:n.1445G>A
ENST00000692792.1:n.761G>A
ENST00000361804.5:c.642G>A MANE Select ENSP00000354720.5:p.Gln214=
ENST00000361804.4:c.642G>A ENSP00000354720.4:p.Gln214=
NM_005445.3:c.642G>A , LRG_774t1:c.642G>A NP_005436.1:p.Gln214=
NM_005445.4:c.642G>A MANE Select NP_005436.1:p.Gln214=