Canonical Allele Identifier: CA2610887768
Gene: SMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1861388205
gnomAD v4: 10-110601601-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110601601G>C , CM000672.2:g.110601601G>C GRCh38
NC_000010.10:g.112361359G>C , CM000672.1:g.112361359G>C GRCh37
NC_000010.9:g.112351349G>C NCBI36
NG_012217.1:g.38911G>C , LRG_774:g.38911G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684988.1:n.4878-36G>C
ENST00000685743.1:n.2317G>C
ENST00000686057.1:n.996-36G>C
ENST00000689321.1:n.1608-36G>C
ENST00000689986.1:n.434-36G>C
ENST00000361804.5:c.2645-36G>C MANE Select ENSP00000354720.5:n.2645-36G>C
ENST00000361804.4:c.2645-36G>C ENSP00000354720.4:n.2645-36G>C
NM_005445.3:c.2645-36G>C , LRG_774t1:c.2645-36G>C NP_005436.1:n.2645-36G>C
NM_005445.4:c.2645-36G>C MANE Select NP_005436.1:n.2645-36G>C
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