Canonical Allele Identifier: CA632123721

Gene: MIR23AHG

Linked Data

• dbSNP Id: rs1458181217
• gnomAD v2: 19-13947200-C-T
• gnomAD v4: 19-13836386-C-T
• MyVariant Identifiers: chr19:g.13947200C>T (hg19) ; chr19:g.13836386C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13836386C>T , CM000681.2:g.13836386C>T	GRCh38
NC_000019.9:g.13947200C>T , CM000681.1:g.13947200C>T	GRCh37
NC_000019.8:g.13808200C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_036515.2:n.6533G>A