Canonical Allele Identifier: CA662845732
Gene: MIR1915HG HGNC NCBI

Linked Data

dbSNP Id: rs1274125340
gnomAD v4: 10-21494713-T-C
MyVariant Identifiers: chr10:g.21783642T>C (hg19) chr10:g.21494713T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494713T>C , CM000672.2:g.21494713T>C GRCh38
NC_000010.10:g.21783642T>C , CM000672.1:g.21783642T>C GRCh37
NC_000010.9:g.21823648T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*887A>G ENSP00000366317.5:n.*887A>G
NM_001010911.2:c.*887A>G NP_001010911.1:n.*887A>G
NM_001010911.3:c.*887A>G NP_001010911.1:n.*887A>G
NR_160800.1:n.1744A>G
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