Canonical Allele Identifier: CA662845726
Gene: MIR1915HG HGNC NCBI

Linked Data

dbSNP Id: rs1337624963
gnomAD v3: 10-21494710-GGGTCTGACCCCGCGC-G
gnomAD v4: 10-21494710-GGGTCTGACCCCGCGC-G
MyVariant Identifiers: chr10:g.21783640_21783654del (hg19) chr10:g.21494711_21494725del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494713_21494727del , CM000672.2:g.21494713_21494727del GRCh38
NC_000010.10:g.21783642_21783656del , CM000672.1:g.21783642_21783656del GRCh37
NC_000010.9:g.21823648_21823662del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*875_*889del ENSP00000366317.5:n.*875_*889del
NM_001010911.2:c.*875_*889del NP_001010911.1:n.*875_*889del
NM_001010911.3:c.*875_*889del NP_001010911.1:n.*875_*889del
NR_160800.1:n.1732_1746del
Search 100 bp 5'
Search 100 bp 3'