Canonical Allele Identifier: CA227368087

Gene: WTAPP1

Linked Data

• dbSNP Id: rs922841888
• MyVariant Identifiers: chr11:g.102669263A>C (hg19) ; chr11:g.102798532A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798532A>C , CM000673.2:g.102798532A>C	GRCh38
NC_000011.9:g.102669263A>C , CM000673.1:g.102669263A>C	GRCh37
NC_000011.8:g.102174473A>C	NCBI36
NG_011740.1:g.4704T>G
NG_011740.2:g.4704T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+410A>C
ENST00000525739.6:n.682+410A>C
ENST00000544704.1:n.443+410A>C
NR_038390.1:n.682+410A>C