Canonical Allele Identifier: CA283979002
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs777739670

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73467565C>A , CM000678.2:g.73467565C>A GRCh38
NC_000016.9:g.73501464C>A , CM000678.1:g.73501464C>A GRCh37
NC_000016.8:g.72058965C>A NCBI36
NG_013211.2:g.429367G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000641206.2:c.-1546-11307G>T ENSP00000493252.1:n.-1546-11307G>T
XM_024450275.1:c.-493-11307G>T XP_024306043.1:n.-493-11307G>T
NM_001386735.1:c.-1063-11307G>T NP_001373664.1:n.-1063-11307G>T