Canonical Allele Identifier: CA2615729020
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134371676
gnomAD v4: 11-102798301-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798301G>T , CM000673.2:g.102798301G>T GRCh38
NC_000011.9:g.102669032G>T , CM000673.1:g.102669032G>T GRCh37
NC_000011.8:g.102174242G>T NCBI36
NG_011740.1:g.4935C>A
NG_011740.2:g.4935C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+179G>T
ENST00000525739.6:n.682+179G>T
ENST00000544704.1:n.443+179G>T
NR_038390.1:n.682+179G>T
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