Canonical Allele Identifier: CA227367997

Gene: WTAPP1

Linked Data

• dbSNP Id: rs778186331
• gnomAD v2: 11-102669120-T-A
• gnomAD v3: 11-102798389-T-A
• gnomAD v4: 11-102798389-T-A
• MyVariant Identifiers: chr11:g.102669120T>A (hg19) ; chr11:g.102798389T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798389T>A , CM000673.2:g.102798389T>A	GRCh38
NC_000011.9:g.102669120T>A , CM000673.1:g.102669120T>A	GRCh37
NC_000011.8:g.102174330T>A	NCBI36
NG_011740.1:g.4847A>T
NG_011740.2:g.4847A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+267T>A
ENST00000525739.6:n.682+267T>A
ENST00000544704.1:n.443+267T>A
NR_038390.1:n.682+267T>A