ClinGen Allele Registry
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Canonical Allele Identifier:
CA763556359
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203874224T>C
GRCh37
chr2:g.204738947T>C
Linked Data - Sequence & Population
gnomAD v3:
2:203874224 T / C
gnomAD v4:
chr2-203874224-T-C
Linked Data - NCBI & NCI
dbSNP:
1377768095
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874224T>C , CM000664.2:g.203874224T>C
GRCh38
NC_000002.11:g.204738947T>C , CM000664.1:g.204738947T>C
GRCh37
NC_000002.10:g.204447192T>C
NCBI36
NG_011502.1:g.11439T>C
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