Canonical Allele Identifier: CA595711426

Gene: SMC3

Linked Data

• dbSNP Id: rs1426934911
• gnomAD v2: 10-112333283-A-C
• gnomAD v3: 10-110573525-A-C
• gnomAD v4: 10-110573525-A-C
• MyVariant Identifiers: chr10:g.112333283A>C (hg19) ; chr10:g.110573525A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110573525A>C , CM000672.2:g.110573525A>C	GRCh38
NC_000010.10:g.112333283A>C , CM000672.1:g.112333283A>C	GRCh37
NC_000010.9:g.112323273A>C	NCBI36
NG_012217.1:g.10835A>C , LRG_774:g.10835A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.225-182A>C
ENST00000687823.1:n.45-1811A>C
ENST00000689932.1:n.383A>C
ENST00000691297.1:n.225-182A>C
ENST00000691527.1:n.182-182A>C
ENST00000692792.1:n.211-182A>C
ENST00000361804.5:c.92-182A>C MANE Select	ENSP00000354720.5:n.92-182A>C
ENST00000361804.4:c.92-182A>C	ENSP00000354720.4:n.92-182A>C
ENST00000462899.1:n.238-182A>C
NM_005445.3:c.92-182A>C , LRG_774t1:c.92-182A>C	NP_005436.1:n.92-182A>C
NM_005445.4:c.92-182A>C MANE Select	NP_005436.1:n.92-182A>C