Canonical Allele Identifier: CA723661400
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs1429539446
gnomAD v3: 16-73679614-C-A
gnomAD v4: 16-73679614-C-A
MyVariant Identifiers: chr16:g.73713513C>A (hg19) chr16:g.73679614C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679614C>A , CM000678.2:g.73679614C>A GRCh38
NC_000016.9:g.73713513C>A , CM000678.1:g.73713513C>A GRCh37
NC_000016.8:g.72271014C>A NCBI36
NG_013211.2:g.217318G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.727G>T
ENST00000641206.2:c.-1547+566G>T ENSP00000493252.1:n.-1547+566G>T
ENST00000642085.1:n.163+566G>T
XR_933730.1:n.355+566G>T
XM_024450275.1:c.-494+566G>T XP_024306043.1:n.-494+566G>T
NM_001386735.1:c.-1064+566G>T NP_001373664.1:n.-1064+566G>T
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