Canonical Allele Identifier: CA925742561
Gene: MIR1915HG HGNC NCBI

Linked Data

dbSNP Id: rs2031795105
gnomAD v3: 10-21494707-G-A
gnomAD v4: 10-21494707-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494707G>A , CM000672.2:g.21494707G>A GRCh38
NC_000010.10:g.21783636G>A , CM000672.1:g.21783636G>A GRCh37
NC_000010.9:g.21823642G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*893C>T ENSP00000366317.5:n.*893C>T
NM_001010911.2:c.*893C>T NP_001010911.1:n.*893C>T
NM_001010911.3:c.*893C>T NP_001010911.1:n.*893C>T
NR_160800.1:n.1750C>T
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