ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA101676593
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.99353060G>T
GRCh37
chr4:g.100274217G>T
Linked Data - Sequence & Population
gnomAD v3:
4:99353060 G / T
gnomAD v4:
chr4-99353060-G-T
Linked Data - NCBI & NCI
dbSNP:
1008981697
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99353060G>T , CM000666.2:g.99353060G>T
GRCh38
NC_000004.11:g.100274217G>T , CM000666.1:g.100274217G>T
GRCh37
NC_000004.10:g.100493240G>T
NCBI36
NG_011718.1:g.4701C>A
Search 100 bp 5'
Search 100 bp 3'