ClinGen Allele Registry
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Canonical Allele Identifier:
CA694637108
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.105545808G>A
GRCh37
chr13:g.106198157G>A
Linked Data - Sequence & Population
gnomAD v3:
13:105545808 G / A
gnomAD v4:
chr13-105545808-G-A
Linked Data - NCBI & NCI
dbSNP:
1268525189
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.105545808G>A , CM000675.2:g.105545808G>A
GRCh38
NC_000013.10:g.106198157G>A , CM000675.1:g.106198157G>A
GRCh37
NC_000013.9:g.104996158G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'