Canonical Allele Identifier: CA723661527
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs1453917284
gnomAD v3: 16-73679922-C-T
gnomAD v4: 16-73679922-C-T
MyVariant Identifiers: chr16:g.73713821C>T (hg19) chr16:g.73679922C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679922C>T , CM000678.2:g.73679922C>T GRCh38
NC_000016.9:g.73713821C>T , CM000678.1:g.73713821C>T GRCh37
NC_000016.8:g.72271322C>T NCBI36
NG_013211.2:g.217010G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.419G>A
ENST00000641206.2:c.-1547+258G>A ENSP00000493252.1:n.-1547+258G>A
ENST00000642085.1:n.163+258G>A
XR_933730.1:n.355+258G>A
XM_024450275.1:c.-494+258G>A XP_024306043.1:n.-494+258G>A
NM_001386735.1:c.-1064+258G>A NP_001373664.1:n.-1064+258G>A
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