Canonical Allele Identifier: CA863494643
Gene: PHF24 HGNC NCBI

Linked Data

dbSNP Id: rs1211346897
gnomAD v2: 9-34825245-G-A
gnomAD v3: 9-34825248-G-A
gnomAD v4: 9-34825248-G-A
MyVariant Identifiers: chr9:g.34825245G>A (hg19) chr9:g.34825248G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34825248G>A , CM000671.2:g.34825248G>A GRCh38
NC_000009.11:g.34825245G>A , CM000671.1:g.34825245G>A GRCh37
NC_000009.10:g.34815245G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011517827.1:c.-66+15089G>A XP_011516129.1:n.-66+15089G>A
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