Canonical Allele Identifier: CA1538249983
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs1754065282
gnomAD v4: 5-34008159-TTTGCGGGCCTGCGCA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008160_34008174del , CM000667.2:g.34008160_34008174del GRCh38
NC_000005.9:g.34008265_34008279del , CM000667.1:g.34008265_34008279del GRCh37
NC_000005.8:g.34044022_34044036del NCBI36
NG_016211.1:g.4942_4956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2275_690-2261del ENSP00000371511.3:n.690-2275_690-2261del
NR_037951.1:n.765-2275_765-2261del
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