Canonical Allele Identifier: CA601246165

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1224152552
• gnomAD v2: 11-102669190-C-G
• gnomAD v3: 11-102798459-C-G
• gnomAD v4: 11-102798459-C-G
• MyVariant Identifiers: chr11:g.102669190C>G (hg19) ; chr11:g.102798459C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798459C>G , CM000673.2:g.102798459C>G	GRCh38
NC_000011.9:g.102669190C>G , CM000673.1:g.102669190C>G	GRCh37
NC_000011.8:g.102174400C>G	NCBI36
NG_011740.1:g.4777G>C
NG_011740.2:g.4777G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+337C>G
ENST00000525739.6:n.682+337C>G
ENST00000544704.1:n.443+337C>G
NR_038390.1:n.682+337C>G