Canonical Allele Identifier: CA662845754
Gene: MIR1915HG HGNC NCBI

Linked Data

dbSNP Id: rs1316279090
gnomAD v3: 10-21494721-C-T
gnomAD v4: 10-21494721-C-T
MyVariant Identifiers: chr10:g.21783650C>T (hg19) chr10:g.21494721C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494721C>T , CM000672.2:g.21494721C>T GRCh38
NC_000010.10:g.21783650C>T , CM000672.1:g.21783650C>T GRCh37
NC_000010.9:g.21823656C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*879G>A ENSP00000366317.5:n.*879G>A
NM_001010911.2:c.*879G>A NP_001010911.1:n.*879G>A
NM_001010911.3:c.*879G>A NP_001010911.1:n.*879G>A
NR_160800.1:n.1736G>A
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