ClinGen Allele Registry
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Canonical Allele Identifier:
CA612030463
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.101417809T>G
GRCh37
chr13:g.102070160T>G
Linked Data - Sequence & Population
gnomAD v2:
13:102070160 T / G
gnomAD v3:
13:101417809 T / G
gnomAD v4:
chr13-101417809-T-G
Linked Data - NCBI & NCI
dbSNP:
2152324
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.101417809T>G , CM000675.2:g.101417809T>G
GRCh38
NC_000013.10:g.102070160T>G , CM000675.1:g.102070160T>G
GRCh37
NC_000013.9:g.100868161T>G
NCBI36
NG_053176.1:g.4398A>C
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