ClinGen Allele Registry
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Canonical Allele Identifier:
CA712620522
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856463T>C
GRCh37
chr15:g.39148664T>C
Linked Data - Sequence & Population
gnomAD v3:
15:38856463 T / C
gnomAD v4:
chr15-38856463-T-C
Linked Data - NCBI & NCI
dbSNP:
1224593128
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856463T>C , CM000677.2:g.38856463T>C
GRCh38
NC_000015.9:g.39148664T>C , CM000677.1:g.39148664T>C
GRCh37
NC_000015.8:g.36935956T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'