Canonical Allele Identifier: CA978940321
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2018594349
gnomAD v3: 16-73467542-A-G
gnomAD v4: 16-73467542-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73467542A>G , CM000678.2:g.73467542A>G GRCh38
NC_000016.9:g.73501441A>G , CM000678.1:g.73501441A>G GRCh37
NC_000016.8:g.72058942A>G NCBI36
NG_013211.2:g.429390T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000641206.2:c.-1546-11284T>C ENSP00000493252.1:n.-1546-11284T>C
XM_024450275.1:c.-493-11284T>C XP_024306043.1:n.-493-11284T>C
NM_001386735.1:c.-1063-11284T>C NP_001373664.1:n.-1063-11284T>C
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