ClinGen Allele Registry
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Canonical Allele Identifier:
CA148990760
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.148602653G>T
GRCh37
chr6:g.148923789G>T
Linked Data - Sequence & Population
gnomAD v2:
6:148923789 G / T
gnomAD v3:
6:148602653 G / T
gnomAD v4:
chr6-148602653-G-T
Joint Max Group AF
0.16115074 (NFE)
Genomes Max Group AF
0.16115074 (NFE)
Linked Data - NCBI & NCI
dbSNP:
13196614
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.148602653G>T , CM000668.2:g.148602653G>T
GRCh38
NC_000006.11:g.148923789G>T , CM000668.1:g.148923789G>T
GRCh37
NC_000006.10:g.148965482G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'