Canonical Allele Identifier: CA1123158810
Gene: PHF24 HGNC NCBI

Linked Data

dbSNP Id: rs1823174983
gnomAD v3: 9-34825221-C-T
gnomAD v4: 9-34825221-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34825221C>T , CM000671.2:g.34825221C>T GRCh38
NC_000009.11:g.34825218C>T , CM000671.1:g.34825218C>T GRCh37
NC_000009.10:g.34815218C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011517827.1:c.-66+15062C>T XP_011516129.1:n.-66+15062C>T