ClinGen Allele Registry
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Canonical Allele Identifier:
CA124378741
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.104872325G>T
GRCh37
chr5:g.104208026G>T
Linked Data - Sequence & Population
gnomAD v3:
5:104872325 G / T
gnomAD v4:
chr5-104872325-G-T
Linked Data - NCBI & NCI
dbSNP:
992010208
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.104872325G>T , CM000667.2:g.104872325G>T
GRCh38
NC_000005.9:g.104208026G>T , CM000667.1:g.104208026G>T
GRCh37
NC_000005.8:g.104235925G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'