Canonical Allele Identifier: CA978947816
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2052990483
gnomAD v3: 16-73679693-A-T
gnomAD v4: 16-73679693-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679693A>T , CM000678.2:g.73679693A>T GRCh38
NC_000016.9:g.73713592A>T , CM000678.1:g.73713592A>T GRCh37
NC_000016.8:g.72271093A>T NCBI36
NG_013211.2:g.217239T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.648T>A
ENST00000641206.2:c.-1547+487T>A ENSP00000493252.1:n.-1547+487T>A
ENST00000642085.1:n.163+487T>A
XR_933730.1:n.355+487T>A
XM_024450275.1:c.-494+487T>A XP_024306043.1:n.-494+487T>A
NM_001386735.1:c.-1064+487T>A NP_001373664.1:n.-1064+487T>A
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