ClinGen Allele Registry
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Canonical Allele Identifier:
CA11146286
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.14926053C>T
GRCh37
chr2:g.15066177C>T
Linked Data - Sequence & Population
gnomAD v2:
2:15066177 C / T
gnomAD v3:
2:14926053 C / T
gnomAD v4:
chr2-14926053-C-T
Joint Max Group AF
0.14864779 (AFR)
Genomes Max Group AF
0.14864779 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1568282
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.14926053C>T , CM000664.2:g.14926053C>T
GRCh38
NC_000002.11:g.15066177C>T , CM000664.1:g.15066177C>T
GRCh37
NC_000002.10:g.14983628C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_922818.1:n.205-146906G>A
Search 100 bp 5'
Search 100 bp 3'