Canonical Allele Identifier: CA670876329

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1363156161
• gnomAD v3: 11-102798391-G-A
• gnomAD v4: 11-102798391-G-A
• MyVariant Identifiers: chr11:g.102669122G>A (hg19) ; chr11:g.102798391G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798391G>A , CM000673.2:g.102798391G>A	GRCh38
NC_000011.9:g.102669122G>A , CM000673.1:g.102669122G>A	GRCh37
NC_000011.8:g.102174332G>A	NCBI36
NG_011740.1:g.4845C>T
NG_011740.2:g.4845C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+269G>A
ENST00000525739.6:n.682+269G>A
ENST00000544704.1:n.443+269G>A
NR_038390.1:n.682+269G>A