Canonical Allele Identifier: CA558971245
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs1244226538
gnomAD v2: 5-34008250-A-AC
gnomAD v3: 5-34008145-A-AC
gnomAD v4: 5-34008145-A-AC
MyVariant Identifiers: chr5:g.34008250_34008251insC (hg19) chr5:g.34008145_34008146insC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008150dup , CM000667.2:g.34008150dup GRCh38
NC_000005.9:g.34008255dup , CM000667.1:g.34008255dup GRCh37
NC_000005.8:g.34044012dup NCBI36
NG_016211.1:g.4970dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2247dup ENSP00000371511.3:n.690-2247dup
NR_037951.1:n.765-2247dup
Search 100 bp 5'
Search 100 bp 3'