ClinGen Allele Registry
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Canonical Allele Identifier:
CA61236553
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.175375121G>A
GRCh37
chr2:g.176239849G>A
Linked Data - Sequence & Population
gnomAD v2:
2:176239849 G / A
gnomAD v3:
2:175375121 G / A
gnomAD v4:
chr2-175375121-G-A
Joint Max Group AF
0.50200147 (AFR)
Genomes Max Group AF
0.50200147 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4972755
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.175375121G>A , CM000664.2:g.175375121G>A
GRCh38
NC_000002.11:g.176239849G>A , CM000664.1:g.176239849G>A
GRCh37
NC_000002.10:g.175948095G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'