Canonical Allele Identifier: CA13394801
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs498186
gnomAD v2: 11-102669645-A-C
gnomAD v3: 11-102798914-A-C
gnomAD v4: 11-102798914-A-C
MyVariant Identifiers: chr11:g.102669645A>C (hg19) chr11:g.102798914A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798914A>C , CM000673.2:g.102798914A>C GRCh38
NC_000011.9:g.102669645A>C , CM000673.1:g.102669645A>C GRCh37
NC_000011.8:g.102174855A>C NCBI36
NG_011740.1:g.4322T>G
NG_011740.2:g.4322T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.423+792A>C
ENST00000525739.6:n.682+792A>C
ENST00000544704.1:n.443+792A>C
NR_038390.1:n.682+792A>C
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