ClinGen Allele Registry
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Canonical Allele Identifier:
CA274663205
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.90350436C>T
GRCh37
chr15:g.90893668C>T
Linked Data - Sequence & Population
gnomAD v3:
15:90350436 C / T
gnomAD v4:
chr15-90350436-C-T
Linked Data - NCBI & NCI
dbSNP:
6496667
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.90350436C>T , CM000677.2:g.90350436C>T
GRCh38
NC_000015.9:g.90893668C>T , CM000677.1:g.90893668C>T
GRCh37
NC_000015.8:g.88694672C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'