Canonical Allele Identifier: CA13394800

Gene: WTAPP1

Linked Data

• ClinVar Variation Id: 1229767
• ClinVar RCV Id: RCV001612115
• dbSNP Id: rs1144393
• gnomAD v2: 11-102669409-T-C
• gnomAD v3: 11-102798678-T-C
• gnomAD v4: 11-102798678-T-C
• MyVariant Identifiers: chr11:g.102669409T>C (hg19) ; chr11:g.102798678T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798678T>C , CM000673.2:g.102798678T>C	GRCh38
NC_000011.9:g.102669409T>C , CM000673.1:g.102669409T>C	GRCh37
NC_000011.8:g.102174619T>C	NCBI36
NG_011740.1:g.4558A>G
NG_011740.2:g.4558A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+556T>C
ENST00000525739.6:n.682+556T>C
ENST00000544704.1:n.443+556T>C
NR_038390.1:n.682+556T>C