Canonical Allele Identifier: CA284007772
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs992837978
gnomAD v2: 16-73713848-T-G
gnomAD v3: 16-73679949-T-G
gnomAD v4: 16-73679949-T-G
MyVariant Identifiers: chr16:g.73713848T>G (hg19) chr16:g.73679949T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679949T>G , CM000678.2:g.73679949T>G GRCh38
NC_000016.9:g.73713848T>G , CM000678.1:g.73713848T>G GRCh37
NC_000016.8:g.72271349T>G NCBI36
NG_013211.2:g.216983A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.392A>C
ENST00000641206.2:c.-1547+231A>C ENSP00000493252.1:n.-1547+231A>C
ENST00000642085.1:n.163+231A>C
XR_933730.1:n.355+231A>C
XM_024450275.1:c.-494+231A>C XP_024306043.1:n.-494+231A>C
NM_001386735.1:c.-1064+231A>C NP_001373664.1:n.-1064+231A>C
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