Canonical Allele Identifier: CA2673482002
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008109-ACGCCCCCAGCCGCGGCGC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008113_34008130del , CM000667.2:g.34008113_34008130del GRCh38
NC_000005.9:g.34008218_34008235del , CM000667.1:g.34008218_34008235del GRCh37
NC_000005.8:g.34043975_34043992del NCBI36
NG_016211.1:g.4989_5006del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2228_690-2211del ENSP00000371511.3:n.690-2228_690-2211del
NR_037951.1:n.765-2228_765-2211del
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