Canonical Allele Identifier: CA283990148
Gene: ZFHX3 HGNC NCBI
MyVariant.info:
GRCh38 chr16:g.73547159A>C
gnomAD v3:
16:73547159 A / C
gnomAD v4:
chr16-73547159-A-C
Joint Max Group AF 0.00000802 (AFR)
Genomes Max Group AF 0.00000802 (AFR)
dbSNP:
7191888
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73547159A>C , CM000678.2:g.73547159A>C GRCh38
NC_000016.9:g.73581058A>C , CM000678.1:g.73581058A>C GRCh37
NC_000016.8:g.72138559A>C NCBI36
NG_013211.2:g.349773T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641206.2:c.-1546-90901T>G ENSP00000493252.1:n.-1546-90901T>G
XM_024450275.1:c.-493-90901T>G XP_024306043.1:n.-493-90901T>G
NM_001386735.1:c.-1063-90901T>G NP_001373664.1:n.-1063-90901T>G
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