Canonical Allele Identifier: CA2480336902
Gene: PRR9 HGNC NCBI

Linked Data

dbSNP Id: rs7534334

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153205376C>A , CM000663.2:g.153205376C>A GRCh38
NC_000001.10:g.153177852C>A , CM000663.1:g.153177852C>A GRCh37
NC_000001.9:g.151444476C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011509806.1:c.-817+65C>A XP_011508108.1:n.-817+65C>A