Canonical Allele Identifier: CA2608488121
Gene: MIR1915HG HGNC NCBI

Linked Data

gnomAD v4: 10-21494607-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494607G>T , CM000672.2:g.21494607G>T GRCh38
NC_000010.10:g.21783536G>T , CM000672.1:g.21783536G>T GRCh37
NC_000010.9:g.21823542G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377113.5:c.*993C>A ENSP00000366317.5:n.*993C>A
NM_001010911.2:c.*993C>A NP_001010911.1:n.*993C>A
NM_001010911.3:c.*993C>A NP_001010911.1:n.*993C>A
NR_160800.1:n.1850C>A
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