Canonical Allele Identifier: CA941631176

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1858263844
• gnomAD v3: 11-102798293-T-C
• gnomAD v4: 11-102798293-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798293T>C , CM000673.2:g.102798293T>C	GRCh38
NC_000011.9:g.102669024T>C , CM000673.1:g.102669024T>C	GRCh37
NC_000011.8:g.102174234T>C	NCBI36
NG_011740.1:g.4943A>G
NG_011740.2:g.4943A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+171T>C
ENST00000525739.6:n.682+171T>C
ENST00000544704.1:n.443+171T>C
NR_038390.1:n.682+171T>C