Canonical Allele Identifier: CA337606168
Gene: ZNF736P9Y HGNC NCBI

Linked Data

dbSNP Id: rs895530
gnomAD v3: Y-8094990-G-T
gnomAD v4: Y-8094990-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8094990G>T , CM000686.2:g.8094990G>T GRCh38
NC_000024.9:g.7963031G>T , CM000686.1:g.7963031G>T GRCh37
NC_000024.8:g.8023031G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000700787.1:n.305+16860C>A
ENST00000651148.1:n.325+16860C>A
XR_938645.1:n.327-652C>A