ClinGen Allele Registry
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Canonical Allele Identifier:
CA146764297
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.120778991G>A
GRCh37
chr6:g.121100137G>A
Linked Data - Sequence & Population
gnomAD v2:
6:121100137 G / A
gnomAD v3:
6:120778991 G / A
gnomAD v4:
chr6-120778991-G-A
Joint Max Group AF
0.12401083 (AFR)
Genomes Max Group AF
0.12401083 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2789066
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.120778991G>A , CM000668.2:g.120778991G>A
GRCh38
NC_000006.11:g.121100137G>A , CM000668.1:g.121100137G>A
GRCh37
NC_000006.10:g.121141836G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'