Canonical Allele Identifier: CA227367902
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs936784476
MyVariant Identifiers: chr11:g.102798291A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798291A>G , CM000673.2:g.102798291A>G GRCh38
NC_000011.9:g.102669022A>G , CM000673.1:g.102669022A>G GRCh37
NC_000011.8:g.102174232A>G NCBI36
NG_011740.1:g.4945T>C
NG_011740.2:g.4945T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+169A>G
ENST00000525739.6:n.682+169A>G
ENST00000544704.1:n.443+169A>G
NR_038390.1:n.682+169A>G
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