ClinGen Allele Registry
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Canonical Allele Identifier:
CA13664778
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.28040056G>A
GRCh37
chr12:g.28192989G>A
Linked Data - Sequence & Population
gnomAD v2:
12:28192989 G / A
gnomAD v3:
12:28040056 G / A
gnomAD v4:
chr12-28040056-G-A
Joint Max Group AF
0.46790675 (AFR)
Genomes Max Group AF
0.46790675 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7964407
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.28040056G>A , CM000674.2:g.28040056G>A
GRCh38
NC_000012.11:g.28192989G>A , CM000674.1:g.28192989G>A
GRCh37
NC_000012.10:g.28084256G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_931460.1:n.154-1098C>T
Search 100 bp 5'
Search 100 bp 3'