Canonical Allele Identifier: CA2673482069
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008161-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008161T>G , CM000667.2:g.34008161T>G GRCh38
NC_000005.9:g.34008266T>G , CM000667.1:g.34008266T>G GRCh37
NC_000005.8:g.34044023T>G NCBI36
NG_016211.1:g.4955A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2262A>C ENSP00000371511.3:n.690-2262A>C
NR_037951.1:n.765-2262A>C
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