Canonical Allele Identifier: CA2673482062
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008156-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008156T>C , CM000667.2:g.34008156T>C GRCh38
NC_000005.9:g.34008261T>C , CM000667.1:g.34008261T>C GRCh37
NC_000005.8:g.34044018T>C NCBI36
NG_016211.1:g.4960A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2257A>G ENSP00000371511.3:n.690-2257A>G
NR_037951.1:n.765-2257A>G
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