Canonical Allele Identifier: CA670868101

Gene: WTAPP1

Linked Data

• dbSNP Id: rs959985848
• gnomAD v3: 11-102785785-C-A
• gnomAD v4: 11-102785785-C-A
• MyVariant Identifiers: chr11:g.102656516C>A (hg19) ; chr11:g.102785785C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102785785C>A , CM000673.2:g.102785785C>A	GRCh38
NC_000011.9:g.102656516C>A , CM000673.1:g.102656516C>A	GRCh37
NC_000011.8:g.102161726C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.325-12239C>A
ENST00000525739.6:n.389+1721C>A
ENST00000544704.1:n.344+1721C>A
NR_038390.1:n.389+1721C>A