Canonical Allele Identifier: CA1895702158
Gene: MIR1915HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494705G= , CM000672.2:g.21494705G= GRCh38
NC_000010.10:g.21783634G= , CM000672.1:g.21783634G= GRCh37
NC_000010.9:g.21823640G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*895C= ENSP00000366317.5:n.*895C=
NM_001010911.2:c.*895C= NP_001010911.1:n.*895C=
NM_001010911.3:c.*895C= NP_001010911.1:n.*895C=
NR_160800.1:n.1752C=