ClinGen Allele Registry
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Canonical Allele Identifier:
CA9243198
Gene: MIR23AHG
HGNC
NCBI
Linked Data
dbSNP Id:
rs376998232
ExAC:
19:13947248 G / A
gnomAD v2:
19-13947248-G-A
gnomAD v3:
19-13836434-G-A
gnomAD v4:
19-13836434-G-A
MyVariant Identifiers:
chr19:g.13947248G>A (hg19)
chr19:g.13836434G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.13836434G>A , CM000681.2:g.13836434G>A
GRCh38
NC_000019.9:g.13947248G>A , CM000681.1:g.13947248G>A
GRCh37
NC_000019.8:g.13808248G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_036515.2:n.6485C>T
Search 100 bp 5'
Search 100 bp 3'