ClinGen Allele Registry
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Canonical Allele Identifier:
CA763556320
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203874142G>A
GRCh37
chr2:g.204738865G>A
Linked Data - Sequence & Population
gnomAD v3:
2:203874142 G / A
gnomAD v4:
chr2-203874142-G-A
Linked Data - NCBI & NCI
dbSNP:
1427942335
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874142G>A , CM000664.2:g.203874142G>A
GRCh38
NC_000002.11:g.204738865G>A , CM000664.1:g.204738865G>A
GRCh37
NC_000002.10:g.204447110G>A
NCBI36
NG_011502.1:g.11357G>A
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