Canonical Allele Identifier: CA2232382220
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2052991892
gnomAD v4: 16-73679816-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679816T>C , CM000678.2:g.73679816T>C GRCh38
NC_000016.9:g.73713715T>C , CM000678.1:g.73713715T>C GRCh37
NC_000016.8:g.72271216T>C NCBI36
NG_013211.2:g.217116A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.525A>G
ENST00000641206.2:c.-1547+364A>G ENSP00000493252.1:n.-1547+364A>G
ENST00000642085.1:n.163+364A>G
XR_933730.1:n.355+364A>G
XM_024450275.1:c.-494+364A>G XP_024306043.1:n.-494+364A>G
NM_001386735.1:c.-1064+364A>G NP_001373664.1:n.-1064+364A>G
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