Canonical Allele Identifier: CA2615728991
Gene: WTAPP1 HGNC NCBI

Linked Data

gnomAD v4: 11-102798248-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798248C>T , CM000673.2:g.102798248C>T GRCh38
NC_000011.9:g.102668979C>T , CM000673.1:g.102668979C>T GRCh37
NC_000011.8:g.102174189C>T NCBI36
NG_011740.1:g.4988G>A
NG_011740.2:g.4988G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+126C>T
ENST00000525739.6:n.682+126C>T
ENST00000544704.1:n.443+126C>T
NR_038390.1:n.682+126C>T
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