Canonical Allele Identifier: CA227367925

Gene: WTAPP1

Linked Data

• dbSNP Id: rs781064763
• MyVariant Identifiers: chr11:g.102669048T>C (hg19) ; chr11:g.102798317T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798317T>C , CM000673.2:g.102798317T>C	GRCh38
NC_000011.9:g.102669048T>C , CM000673.1:g.102669048T>C	GRCh37
NC_000011.8:g.102174258T>C	NCBI36
NG_011740.1:g.4919A>G
NG_011740.2:g.4919A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+195T>C
ENST00000525739.6:n.682+195T>C
ENST00000544704.1:n.443+195T>C
NR_038390.1:n.682+195T>C