Canonical Allele Identifier: CA283970284
Gene: ZFHX3 HGNC NCBI
LOHAN2 HGNC NCBI

Linked Data

dbSNP Id: rs9934948
gnomAD v2: 16-73439355-C-T
gnomAD v3: 16-73405456-C-T
gnomAD v4: 16-73405456-C-T
MyVariant Identifiers: chr16:g.73439355C>T (hg19) chr16:g.73405456C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73405456C>T , CM000678.2:g.73405456C>T GRCh38
NC_000016.9:g.73439355C>T , CM000678.1:g.73439355C>T GRCh37
NC_000016.8:g.71996856C>T NCBI36
NG_013211.2:g.491476G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000641206.2:c.-1291+50547G>A (ZFHX3) ENSP00000493252.1:n.-1291+50547G>A
NR_038234.1:n.451-14637C>T (LOHAN2)
XM_024450275.1:c.-238+50547G>A XP_024306043.1:n.-238+50547G>A
NM_001386735.1:c.-808+50547G>A (ZFHX3) NP_001373664.1:n.-808+50547G>A
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