ClinGen Allele Registry
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Canonical Allele Identifier:
CA568658042
Gene: UFL1-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1367718757
gnomAD v2:
6-96860585-A-C
gnomAD v3:
6-96412709-A-C
gnomAD v4:
6-96412709-A-C
MyVariant Identifiers:
chr6:g.96860585A>C (hg19)
chr6:g.96412709A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.96412709A>C , CM000668.2:g.96412709A>C
GRCh38
NC_000006.11:g.96860585A>C , CM000668.1:g.96860585A>C
GRCh37
NC_000006.10:g.96967306A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_002956363.1:n.9203-43229T>G
Search 100 bp 5'
Search 100 bp 3'