Canonical Allele Identifier: CA10865040
Gene: PRR9 HGNC NCBI

Linked Data

dbSNP Id: rs7534334

Genomic Alleles

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

Transcript Alleles

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