Canonical Allele Identifier: CA2673482042
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008142-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008142A>T , CM000667.2:g.34008142A>T GRCh38
NC_000005.9:g.34008247A>T , CM000667.1:g.34008247A>T GRCh37
NC_000005.8:g.34044004A>T NCBI36
NG_016211.1:g.4974T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2243T>A ENSP00000371511.3:n.690-2243T>A
NR_037951.1:n.765-2243T>A