Canonical Allele Identifier: CA809989450
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs1460199118
gnomAD v4: 5-34008128-C-T
MyVariant Identifiers: chr5:g.34008233C>T (hg19) chr5:g.34008128C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008128C>T , CM000667.2:g.34008128C>T GRCh38
NC_000005.9:g.34008233C>T , CM000667.1:g.34008233C>T GRCh37
NC_000005.8:g.34043990C>T NCBI36
NG_016211.1:g.4988G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2229G>A ENSP00000371511.3:n.690-2229G>A
NR_037951.1:n.765-2229G>A
Search 100 bp 5'
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