ClinGen Allele Registry
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Canonical Allele Identifier:
CA15776035
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.65907683G>T
GRCh37
chr13:g.66481815G>T
Linked Data - Sequence & Population
gnomAD v2:
13:66481815 G / T
gnomAD v3:
13:65907683 G / T
gnomAD v4:
chr13-65907683-G-T
Joint Max Group AF
0.39861098 (SAS)
Genomes Max Group AF
0.39861098 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1585440
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.65907683G>T , CM000675.2:g.65907683G>T
GRCh38
NC_000013.10:g.66481815G>T , CM000675.1:g.66481815G>T
GRCh37
NC_000013.9:g.65379816G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_942033.1:n.138+3457G>T
Search 100 bp 5'
Search 100 bp 3'