Canonical Allele Identifier: CA1895702170
Gene: MIR1915HG HGNC NCBI

Linked Data

dbSNP Id: rs2031795369
gnomAD v3: 10-21494722-G-A
gnomAD v4: 10-21494722-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494722G>A , CM000672.2:g.21494722G>A GRCh38
NC_000010.10:g.21783651G>A , CM000672.1:g.21783651G>A GRCh37
NC_000010.9:g.21823657G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*878C>T ENSP00000366317.5:n.*878C>T
NM_001010911.2:c.*878C>T NP_001010911.1:n.*878C>T
NM_001010911.3:c.*878C>T NP_001010911.1:n.*878C>T
NR_160800.1:n.1735C>T
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