Canonical Allele Identifier: CA2615729023
Gene: WTAPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798308T>C , CM000673.2:g.102798308T>C GRCh38
NC_000011.9:g.102669039T>C , CM000673.1:g.102669039T>C GRCh37
NC_000011.8:g.102174249T>C NCBI36
NG_011740.1:g.4928A>G
NG_011740.2:g.4928A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+186T>C
ENST00000525739.6:n.682+186T>C
ENST00000544704.1:n.443+186T>C
NR_038390.1:n.682+186T>C