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Canonical Allele Identifier:
CA14897978
Gene: ETS2-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.38911809C>T
GRCh37
chr21:g.40283733C>T
Linked Data - Sequence & Population
gnomAD v2:
21:40283733 C / T
gnomAD v3:
21:38911809 C / T
gnomAD v4:
chr21-38911809-C-T
Joint Max Group AF
0.04495415 (NFE)
Genomes Max Group AF
0.04495415 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9979250
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.38911809C>T , CM000683.2:g.38911809C>T
GRCh38
NC_000021.8:g.40283733C>T , CM000683.1:g.40283733C>T
GRCh37
NC_000021.7:g.39205603C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120405.1:n.677-9844G>A
Search 100 bp 5'
Search 100 bp 3'