Canonical Allele Identifier: CA1123158813
Gene: PHF24 HGNC NCBI

Linked Data

dbSNP Id: rs1823175028
gnomAD v3: 9-34825222-A-C
gnomAD v4: 9-34825222-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34825222A>C , CM000671.2:g.34825222A>C GRCh38
NC_000009.11:g.34825219A>C , CM000671.1:g.34825219A>C GRCh37
NC_000009.10:g.34815219A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011517827.1:c.-66+15063A>C XP_011516129.1:n.-66+15063A>C