Canonical Allele Identifier: CA227367940

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1041701272
• gnomAD v2: 11-102669059-A-G
• gnomAD v3: 11-102798328-A-G
• gnomAD v4: 11-102798328-A-G
• MyVariant Identifiers: chr11:g.102669059A>G (hg19) ; chr11:g.102798328A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798328A>G , CM000673.2:g.102798328A>G	GRCh38
NC_000011.9:g.102669059A>G , CM000673.1:g.102669059A>G	GRCh37
NC_000011.8:g.102174269A>G	NCBI36
NG_011740.1:g.4908T>C
NG_011740.2:g.4908T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371455.7:n.423+206A>G
ENST00000525739.6:n.682+206A>G
ENST00000544704.1:n.443+206A>G
NR_038390.1:n.682+206A>G