ClinGen Allele Registry
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Canonical Allele Identifier:
CA11104001
Gene: TARDBPP3
HGNC
NCBI
Linked Data
dbSNP Id:
rs11689432
gnomAD v2:
2-239141505-A-G
gnomAD v3:
2-238232864-A-G
gnomAD v4:
2-238232864-A-G
MyVariant Identifiers:
chr2:g.239141505A>G (hg19)
chr2:g.238232864A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.238232864A>G , CM000664.2:g.238232864A>G
GRCh38
NC_000002.11:g.239141505A>G , CM000664.1:g.239141505A>G
GRCh37
NC_000002.10:g.238806244A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_026923.1:n.1179A>G
Search 100 bp 5'
Search 100 bp 3'