Canonical Allele Identifier: CA2608488243
Gene: MIR1915HG HGNC NCBI

Linked Data

gnomAD v4: 10-21494708-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494708G>A , CM000672.2:g.21494708G>A GRCh38
NC_000010.10:g.21783637G>A , CM000672.1:g.21783637G>A GRCh37
NC_000010.9:g.21823643G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*892C>T ENSP00000366317.5:n.*892C>T
NM_001010911.2:c.*892C>T NP_001010911.1:n.*892C>T
NM_001010911.3:c.*892C>T NP_001010911.1:n.*892C>T
NR_160800.1:n.1749C>T
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