Canonical Allele Identifier: CA809989472
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs563127635
gnomAD v4: 5-34008164-G-T
MyVariant Identifiers: chr5:g.34008269G>T (hg19) chr5:g.34008164G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008164G>T , CM000667.2:g.34008164G>T GRCh38
NC_000005.9:g.34008269G>T , CM000667.1:g.34008269G>T GRCh37
NC_000005.8:g.34044026G>T NCBI36
NG_016211.1:g.4952C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2265C>A ENSP00000371511.3:n.690-2265C>A
NR_037951.1:n.765-2265C>A
Search 100 bp 5'
Search 100 bp 3'