Canonical Allele Identifier: CA284007771
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs1036323699
gnomAD v3: 16-73679942-G-C
gnomAD v4: 16-73679942-G-C
MyVariant Identifiers: chr16:g.73713841G>C (hg19) chr16:g.73679942G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679942G>C , CM000678.2:g.73679942G>C GRCh38
NC_000016.9:g.73713841G>C , CM000678.1:g.73713841G>C GRCh37
NC_000016.8:g.72271342G>C NCBI36
NG_013211.2:g.216990C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.399C>G
ENST00000641206.2:c.-1547+238C>G ENSP00000493252.1:n.-1547+238C>G
ENST00000642085.1:n.163+238C>G
XR_933730.1:n.355+238C>G
XM_024450275.1:c.-494+238C>G XP_024306043.1:n.-494+238C>G
NM_001386735.1:c.-1064+238C>G NP_001373664.1:n.-1064+238C>G
Search 100 bp 5'
Search 100 bp 3'