Canonical Allele Identifier: CA27775132

Gene: MIR137HG

Linked Data

• dbSNP Id: rs77177281
• gnomAD v2: 1-98471702-A-T
• gnomAD v3: 1-98006146-A-T
• gnomAD v4: 1-98006146-A-T
• MyVariant Identifiers: chr1:g.98471702A>T (hg19) ; chr1:g.98006146A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.98006146A>T , CM000663.2:g.98006146A>T	GRCh38
NC_000001.10:g.98471702A>T , CM000663.1:g.98471702A>T	GRCh37
NC_000001.9:g.98244290A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_046105.1:n.815-11146T>A