ClinGen Allele Registry
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Canonical Allele Identifier:
CA150162988
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.151633699A>G
GRCh37
chr6:g.151954834A>G
Linked Data - Sequence & Population
gnomAD v2:
6:151954834 A / G
gnomAD v3:
6:151633699 A / G
gnomAD v4:
chr6-151633699-A-G
Joint Max Group AF
0.10205399 (AMR)
Genomes Max Group AF
0.10205399 (AMR)
Linked Data - NCBI & NCI
dbSNP:
140068132
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.151633699A>G , CM000668.2:g.151633699A>G
GRCh38
NC_000006.11:g.151954834A>G , CM000668.1:g.151954834A>G
GRCh37
NC_000006.10:g.151996527A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_943115.1:n.2496+3717A>G
Search 100 bp 5'
Search 100 bp 3'