ClinGen Allele Registry
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Canonical Allele Identifier:
CA64810994
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.214810169G>A
GRCh37
chr2:g.215674893G>A
Linked Data - Sequence & Population
gnomAD v2:
2:215674893 G / A
gnomAD v3:
2:214810169 G / A
gnomAD v4:
chr2-214810169-G-A
Joint Max Group AF
0.00701639 (EAS)
Genomes Max Group AF
0.00704072 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17426219
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.214810169G>A , CM000664.2:g.214810169G>A
GRCh38
NC_000002.11:g.215674893G>A , CM000664.1:g.215674893G>A
GRCh37
NC_000002.10:g.215383138G>A
NCBI36
NG_012047.2:g.4536C>T
NG_012047.3:g.4543C>T
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