Canonical Allele Identifier: CA284007770
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs949954926
MyVariant Identifiers: chr16:g.73679935A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679935A>G , CM000678.2:g.73679935A>G GRCh38
NC_000016.9:g.73713834A>G , CM000678.1:g.73713834A>G GRCh37
NC_000016.8:g.72271335A>G NCBI36
NG_013211.2:g.216997T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.406T>C
ENST00000641206.2:c.-1547+245T>C ENSP00000493252.1:n.-1547+245T>C
ENST00000642085.1:n.163+245T>C
XR_933730.1:n.355+245T>C
XM_024450275.1:c.-494+245T>C XP_024306043.1:n.-494+245T>C
NM_001386735.1:c.-1064+245T>C NP_001373664.1:n.-1064+245T>C