Canonical Allele Identifier: CA116873333
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs111688000
gnomAD v3: 5-34008122-C-T
gnomAD v4: 5-34008122-C-T
MyVariant Identifiers: chr5:g.34008227C>T (hg19) chr5:g.34008122C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008122C>T , CM000667.2:g.34008122C>T GRCh38
NC_000005.9:g.34008227C>T , CM000667.1:g.34008227C>T GRCh37
NC_000005.8:g.34043984C>T NCBI36
NG_016211.1:g.4994G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2223G>A ENSP00000371511.3:n.690-2223G>A
NR_037951.1:n.765-2223G>A
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