Canonical Allele Identifier: CA227368010

Gene: WTAPP1

Linked Data

• dbSNP Id: rs139305393
• gnomAD v2: 11-102669152-A-G
• gnomAD v3: 11-102798421-A-G
• gnomAD v4: 11-102798421-A-G
• MyVariant Identifiers: chr11:g.102669152A>G (hg19) ; chr11:g.102798421A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798421A>G , CM000673.2:g.102798421A>G	GRCh38
NC_000011.9:g.102669152A>G , CM000673.1:g.102669152A>G	GRCh37
NC_000011.8:g.102174362A>G	NCBI36
NG_011740.1:g.4815T>C
NG_011740.2:g.4815T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+299A>G
ENST00000525739.6:n.682+299A>G
ENST00000544704.1:n.443+299A>G
NR_038390.1:n.682+299A>G