Canonical Allele Identifier: CA601245743

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1465371697
• gnomAD v2: 11-102656501-G-T
• gnomAD v3: 11-102785770-G-T
• gnomAD v4: 11-102785770-G-T
• MyVariant Identifiers: chr11:g.102656501G>T (hg19) ; chr11:g.102785770G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102785770G>T , CM000673.2:g.102785770G>T	GRCh38
NC_000011.9:g.102656501G>T , CM000673.1:g.102656501G>T	GRCh37
NC_000011.8:g.102161711G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.325-12254G>T
ENST00000525739.6:n.389+1706G>T
ENST00000544704.1:n.344+1706G>T
NR_038390.1:n.389+1706G>T