Canonical Allele Identifier: CA27778521
Gene: MIR137HG HGNC NCBI

Linked Data

dbSNP Id: rs1702294
gnomAD v2: 1-98501984-T-C
gnomAD v3: 1-98036428-T-C
gnomAD v4: 1-98036428-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.98036428T>C , CM000663.2:g.98036428T>C GRCh38
NC_000001.10:g.98501984T>C , CM000663.1:g.98501984T>C GRCh37
NC_000001.9:g.98274572T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046105.1:n.814+9580A>G