ClinGen Allele Registry
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Canonical Allele Identifier:
CA536376757
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.134454758G>A
GRCh37
chr2:g.135212329G>A
Linked Data - Sequence & Population
gnomAD v2:
2:135212329 G / A
gnomAD v3:
2:134454758 G / A
gnomAD v4:
chr2-134454758-G-A
Linked Data - NCBI & NCI
dbSNP:
539588
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.134454758G>A , CM000664.2:g.134454758G>A
GRCh38
NC_000002.11:g.135212329G>A , CM000664.1:g.135212329G>A
GRCh37
NC_000002.10:g.134928799G>A
NCBI36
NG_030324.1:g.205500G>A
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