Canonical Allele Identifier: CA14672801
Gene: ZNF98 HGNC NCBI

Linked Data

dbSNP Id: rs10404998

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