Canonical Allele Identifier: CA601246164

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1273010744
• gnomAD v2: 11-102669181-A-G
• gnomAD v3: 11-102798450-A-G
• gnomAD v4: 11-102798450-A-G
• MyVariant Identifiers: chr11:g.102669181A>G (hg19) ; chr11:g.102798450A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798450A>G , CM000673.2:g.102798450A>G	GRCh38
NC_000011.9:g.102669181A>G , CM000673.1:g.102669181A>G	GRCh37
NC_000011.8:g.102174391A>G	NCBI36
NG_011740.1:g.4786T>C
NG_011740.2:g.4786T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+328A>G
ENST00000525739.6:n.682+328A>G
ENST00000544704.1:n.443+328A>G
NR_038390.1:n.682+328A>G