Canonical Allele Identifier: CA2608488256
Gene: MIR1915HG HGNC NCBI

Linked Data

gnomAD v4: 10-21494715-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494715T>C , CM000672.2:g.21494715T>C GRCh38
NC_000010.10:g.21783644T>C , CM000672.1:g.21783644T>C GRCh37
NC_000010.9:g.21823650T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*885A>G ENSP00000366317.5:n.*885A>G
NM_001010911.2:c.*885A>G NP_001010911.1:n.*885A>G
NM_001010911.3:c.*885A>G NP_001010911.1:n.*885A>G
NR_160800.1:n.1742A>G
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