Canonical Allele Identifier: CA227367943
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs980443111
gnomAD v3: 11-102798345-A-C
gnomAD v4: 11-102798345-A-C
MyVariant Identifiers: chr11:g.102669076A>C (hg19) chr11:g.102798345A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798345A>C , CM000673.2:g.102798345A>C GRCh38
NC_000011.9:g.102669076A>C , CM000673.1:g.102669076A>C GRCh37
NC_000011.8:g.102174286A>C NCBI36
NG_011740.1:g.4891T>G
NG_011740.2:g.4891T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+223A>C
ENST00000525739.6:n.682+223A>C
ENST00000544704.1:n.443+223A>C
NR_038390.1:n.682+223A>C
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