Canonical Allele Identifier: CA978940336
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2018595883

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73467652A>T , CM000678.2:g.73467652A>T GRCh38
NC_000016.9:g.73501551A>T , CM000678.1:g.73501551A>T GRCh37
NC_000016.8:g.72059052A>T NCBI36
NG_013211.2:g.429280T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641206.2:c.-1546-11394T>A ENSP00000493252.1:n.-1546-11394T>A
XM_024450275.1:c.-493-11394T>A XP_024306043.1:n.-493-11394T>A
NM_001386735.1:c.-1063-11394T>A NP_001373664.1:n.-1063-11394T>A