Canonical Allele Identifier: CA1845746260
Gene: PHF24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34825219G= , CM000671.2:g.34825219G= GRCh38
NC_000009.11:g.34825216G= , CM000671.1:g.34825216G= GRCh37
NC_000009.10:g.34815216G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011517827.1:c.-66+15060G= XP_011516129.1:n.-66+15060G=