Canonical Allele Identifier: CA1074912561
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs937490547
gnomAD v3: 5-34008109-A-ACGCCCCCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCG
gnomAD v4: 5-34008109-A-ACGCCCCCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008135_34008136insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC , CM000667.2:g.34008135_34008136insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC GRCh38
NC_000005.9:g.34008240_34008241insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC , CM000667.1:g.34008240_34008241insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC GRCh37
NC_000005.8:g.34043997_34043998insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC NCBI36
NG_016211.1:g.5006_5007insCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2211_690-2210insCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCG ENSP00000371511.3:n.690-2211_690-2210insCGGCGCCGCGGCTGGGGGCGC...
NR_037951.1:n.765-2211_765-2210insCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCG
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