Canonical Allele Identifier: CA2673482093
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008185-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008185G>T , CM000667.2:g.34008185G>T GRCh38
NC_000005.9:g.34008290G>T , CM000667.1:g.34008290G>T GRCh37
NC_000005.8:g.34044047G>T NCBI36
NG_016211.1:g.4931C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2286C>A ENSP00000371511.3:n.690-2286C>A
NR_037951.1:n.765-2286C>A