Canonical Allele Identifier: CA13394800
Gene: WTAPP1 HGNC NCBI
gnomAD v2:
11:102669409 T / C
gnomAD v3:
11:102798678 T / C
gnomAD v4:
chr11-102798678-T-C
Joint Max Group AF 0.38382508 (NFE)
Genomes Max Group AF 0.38382508 (NFE)
ClinVar RCV:
RCV001612115
ClinVar Variation:
1229767
dbSNP:
1144393
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798678T>C , CM000673.2:g.102798678T>C GRCh38
NC_000011.9:g.102669409T>C , CM000673.1:g.102669409T>C GRCh37
NC_000011.8:g.102174619T>C NCBI36
NG_011740.1:g.4558A>G
NG_011740.2:g.4558A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+556T>C
ENST00000525739.6:n.682+556T>C
ENST00000544704.1:n.443+556T>C
NR_038390.1:n.682+556T>C
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