Canonical Allele Identifier: CA14672801
Gene: ZNF98 HGNC NCBI
dbSNP:
10404998
gnomAD v2:
19:22608374 T / C
gnomAD v3:
19:22425572 T / C
gnomAD v4:
chr19-22425572-T-C
Joint Max Group AF 0.45695935 (NFE)
Genomes Max Group AF 0.45695935 (NFE)
MyVariant.info:
GRCh38 chr19:g.22425572T>C
GRCh37 chr19:g.22608374T>C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.22425572T>C , CM000681.2:g.22425572T>C GRCh38
NC_000019.9:g.22608374T>C , CM000681.1:g.22608374T>C GRCh37
NC_000019.8:g.22400214T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000593802.1:c.316-22060A>G ENSP00000472301.1:n.316-22060A>G
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