Canonical Allele Identifier: CA2580920888

Gene: MIR1915HG

Genomic Alleles

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

Transcript Alleles

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