ClinGen Allele Registry
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Canonical Allele Identifier:
CA705269042
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.35405317T>C
GRCh37
chr14:g.35874523T>C
Linked Data - Sequence & Population
gnomAD v3:
14:35405317 T / C
gnomAD v4:
chr14-35405317-T-C
Linked Data - NCBI & NCI
dbSNP:
2233407
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.35405317T>C , CM000676.2:g.35405317T>C
GRCh38
NC_000014.8:g.35874523T>C , CM000676.1:g.35874523T>C
GRCh37
NC_000014.7:g.34944274T>C
NCBI36
NG_007571.1:g.4422A>G , LRG_89:g.4422A>G
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