Canonical Allele Identifier: CA227368007

Gene: WTAPP1

Linked Data

• dbSNP Id: rs527647848
• gnomAD v3: 11-102798409-C-A
• gnomAD v4: 11-102798409-C-A
• MyVariant Identifiers: chr11:g.102669140C>A (hg19) ; chr11:g.102798409C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798409C>A , CM000673.2:g.102798409C>A	GRCh38
NC_000011.9:g.102669140C>A , CM000673.1:g.102669140C>A	GRCh37
NC_000011.8:g.102174350C>A	NCBI36
NG_011740.1:g.4827G>T
NG_011740.2:g.4827G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+287C>A
ENST00000525739.6:n.682+287C>A
ENST00000544704.1:n.443+287C>A
NR_038390.1:n.682+287C>A