Canonical Allele Identifier: CA227368092

Gene: WTAPP1

Linked Data

• dbSNP Id: rs564251183
• gnomAD v2: 11-102669291-C-T
• gnomAD v3: 11-102798560-C-T
• gnomAD v4: 11-102798560-C-T
• MyVariant Identifiers: chr11:g.102669291C>T (hg19) ; chr11:g.102798560C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798560C>T , CM000673.2:g.102798560C>T	GRCh38
NC_000011.9:g.102669291C>T , CM000673.1:g.102669291C>T	GRCh37
NC_000011.8:g.102174501C>T	NCBI36
NG_011740.1:g.4676G>A
NG_011740.2:g.4676G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+438C>T
ENST00000525739.6:n.682+438C>T
ENST00000544704.1:n.443+438C>T
NR_038390.1:n.682+438C>T