Canonical Allele Identifier: CA227367896
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs751961954
gnomAD v4: 11-102798266-G-C
MyVariant Identifiers: chr11:g.102668997G>C (hg19) chr11:g.102798266G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798266G>C , CM000673.2:g.102798266G>C GRCh38
NC_000011.9:g.102668997G>C , CM000673.1:g.102668997G>C GRCh37
NC_000011.8:g.102174207G>C NCBI36
NG_011740.1:g.4970C>G
NG_011740.2:g.4970C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+144G>C
ENST00000525739.6:n.682+144G>C
ENST00000544704.1:n.443+144G>C
NR_038390.1:n.682+144G>C
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