Canonical Allele Identifier: CA809989441
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs1442959362
MyVariant Identifiers: chr5:g.34008218_34008236del (hg19) chr5:g.34008113_34008131del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008118_34008136del , CM000667.2:g.34008118_34008136del GRCh38
NC_000005.9:g.34008223_34008241del , CM000667.1:g.34008223_34008241del GRCh37
NC_000005.8:g.34043980_34043998del NCBI36
NG_016211.1:g.4985_5003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2232_690-2214del ENSP00000371511.3:n.690-2232_690-2214del
NR_037951.1:n.765-2232_765-2214del
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