Canonical Allele Identifier: CA2673482079
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008170-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008170G>T , CM000667.2:g.34008170G>T GRCh38
NC_000005.9:g.34008275G>T , CM000667.1:g.34008275G>T GRCh37
NC_000005.8:g.34044032G>T NCBI36
NG_016211.1:g.4946C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2271C>A ENSP00000371511.3:n.690-2271C>A
NR_037951.1:n.765-2271C>A
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