Canonical Allele Identifier: CA284007705
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs899297318
gnomAD v3: 16-73679497-C-G
gnomAD v4: 16-73679497-C-G
MyVariant Identifiers: chr16:g.73713396C>G (hg19) chr16:g.73679497C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679497C>G , CM000678.2:g.73679497C>G GRCh38
NC_000016.9:g.73713396C>G , CM000678.1:g.73713396C>G GRCh37
NC_000016.8:g.72270897C>G NCBI36
NG_013211.2:g.217435G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641206.2:c.-1547+683G>C ENSP00000493252.1:n.-1547+683G>C
ENST00000642085.1:n.163+683G>C
XR_933730.1:n.355+683G>C
XM_024450275.1:c.-494+683G>C XP_024306043.1:n.-494+683G>C
NM_001386735.1:c.-1064+683G>C NP_001373664.1:n.-1064+683G>C
Search 100 bp 5'
Search 100 bp 3'