ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA127211589
Gene: MIR3936HG
HGNC
NCBI
Linked Data
dbSNP Id:
rs10058074
gnomAD v2:
5-131686146-G-A
gnomAD v3:
5-132350453-G-A
gnomAD v4:
5-132350453-G-A
MyVariant Identifiers:
chr5:g.131686146G>A (hg19)
chr5:g.132350453G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.132350453G>A , CM000667.2:g.132350453G>A
GRCh38
NC_000005.9:g.131686146G>A , CM000667.1:g.131686146G>A
GRCh37
NC_000005.8:g.131714045G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_110997.1:n.418-496C>T
Search 100 bp 5'
Search 100 bp 3'