Canonical Allele Identifier: CA284007704
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs1043775658
gnomAD v2: 16-73713382-C-T
gnomAD v3: 16-73679483-C-T
gnomAD v4: 16-73679483-C-T
MyVariant Identifiers: chr16:g.73713382C>T (hg19) chr16:g.73679483C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679483C>T , CM000678.2:g.73679483C>T GRCh38
NC_000016.9:g.73713382C>T , CM000678.1:g.73713382C>T GRCh37
NC_000016.8:g.72270883C>T NCBI36
NG_013211.2:g.217449G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641206.2:c.-1547+697G>A ENSP00000493252.1:n.-1547+697G>A
ENST00000642085.1:n.163+697G>A
XR_933730.1:n.355+697G>A
XM_024450275.1:c.-494+697G>A XP_024306043.1:n.-494+697G>A
NM_001386735.1:c.-1064+697G>A NP_001373664.1:n.-1064+697G>A
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