Canonical Allele Identifier: CA2608488248
Gene: MIR1915HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494711G>A , CM000672.2:g.21494711G>A GRCh38
NC_000010.10:g.21783640G>A , CM000672.1:g.21783640G>A GRCh37
NC_000010.9:g.21823646G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*889C>T ENSP00000366317.5:n.*889C>T
NM_001010911.2:c.*889C>T NP_001010911.1:n.*889C>T
NM_001010911.3:c.*889C>T NP_001010911.1:n.*889C>T
NR_160800.1:n.1746C>T