Canonical Allele Identifier: CA670876297
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1156909133
gnomAD v3: 11-102798315-A-G
gnomAD v4: 11-102798315-A-G
MyVariant Identifiers: chr11:g.102669046A>G (hg19) chr11:g.102798315A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798315A>G , CM000673.2:g.102798315A>G GRCh38
NC_000011.9:g.102669046A>G , CM000673.1:g.102669046A>G GRCh37
NC_000011.8:g.102174256A>G NCBI36
NG_011740.1:g.4921T>C
NG_011740.2:g.4921T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+193A>G
ENST00000525739.6:n.682+193A>G
ENST00000544704.1:n.443+193A>G
NR_038390.1:n.682+193A>G
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