Canonical Allele Identifier: CA2608488242
Gene: MIR1915HG HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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