Canonical Allele Identifier: CA2673482037
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008138-A-AGCCGC
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008139_34008140insCCGCG , CM000667.2:g.34008139_34008140insCCGCG GRCh38
NC_000005.9:g.34008244_34008245insCCGCG , CM000667.1:g.34008244_34008245insCCGCG GRCh37
NC_000005.8:g.34044001_34044002insCCGCG NCBI36
NG_016211.1:g.4977_4978insGCGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2240_690-2239insGCGGC ENSP00000371511.3:n.690-2240_690-2239insGCGGC
NR_037951.1:n.765-2240_765-2239insGCGGC
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