Canonical Allele Identifier: CA2673482058
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008151-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008151G>C , CM000667.2:g.34008151G>C GRCh38
NC_000005.9:g.34008256G>C , CM000667.1:g.34008256G>C GRCh37
NC_000005.8:g.34044013G>C NCBI36
NG_016211.1:g.4965C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2252C>G ENSP00000371511.3:n.690-2252C>G
NR_037951.1:n.765-2252C>G
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