Canonical Allele Identifier: CA1895702167
Gene: MIR1915HG HGNC NCBI

Linked Data

dbSNP Id: rs2031795287
gnomAD v4: 10-21494718-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494718C>A , CM000672.2:g.21494718C>A GRCh38
NC_000010.10:g.21783647C>A , CM000672.1:g.21783647C>A GRCh37
NC_000010.9:g.21823653C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*882G>T ENSP00000366317.5:n.*882G>T
NM_001010911.2:c.*882G>T NP_001010911.1:n.*882G>T
NM_001010911.3:c.*882G>T NP_001010911.1:n.*882G>T
NR_160800.1:n.1739G>T
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