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Canonical Allele Identifier:
CA11037771
Gene: DLX2-DT
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.172108243G>A
GRCh37
chr2:g.172972971G>A
Linked Data - Sequence & Population
gnomAD v2:
2:172972971 G / A
gnomAD v3:
2:172108243 G / A
gnomAD v4:
chr2-172108243-G-A
Joint Max Group AF
0.46760988 (NFE)
Genomes Max Group AF
0.46760988 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2016394
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.172108243G>A , CM000664.2:g.172108243G>A
GRCh38
NC_000002.11:g.172972971G>A , CM000664.1:g.172972971G>A
GRCh37
NC_000002.10:g.172681217G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_126376.1:n.677-659G>A
Search 100 bp 5'
Search 100 bp 3'