ClinGen Allele Registry
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Canonical Allele Identifier:
CA539148192
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203878211G>A
GRCh37
chr2:g.204742934G>A
Linked Data - Sequence & Population
gnomAD v2:
2:204742934 G / A
gnomAD v3:
2:203878211 G / A
gnomAD v4:
chr2-203878211-G-A
Linked Data - NCBI & NCI
dbSNP:
11571302
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203878211G>A , CM000664.2:g.203878211G>A
GRCh38
NC_000002.11:g.204742934G>A , CM000664.1:g.204742934G>A
GRCh37
NC_000002.10:g.204451179G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'