ClinGen Allele Registry
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Canonical Allele Identifier:
CA610765337
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.65907683G>A
GRCh37
chr13:g.66481815G>A
Linked Data - Sequence & Population
gnomAD v2:
13:66481815 G / A
Linked Data - NCBI & NCI
dbSNP:
1585440
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.65907683G>A , CM000675.2:g.65907683G>A
GRCh38
NC_000013.10:g.66481815G>A , CM000675.1:g.66481815G>A
GRCh37
NC_000013.9:g.65379816G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_942033.1:n.138+3457G>A
Search 100 bp 5'
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