Canonical Allele Identifier: CA2608488246
Gene: MIR1915HG HGNC NCBI

Linked Data

gnomAD v4: 10-21494709-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494709T>G , CM000672.2:g.21494709T>G GRCh38
NC_000010.10:g.21783638T>G , CM000672.1:g.21783638T>G GRCh37
NC_000010.9:g.21823644T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*891A>C ENSP00000366317.5:n.*891A>C
NM_001010911.2:c.*891A>C NP_001010911.1:n.*891A>C
NM_001010911.3:c.*891A>C NP_001010911.1:n.*891A>C
NR_160800.1:n.1748A>C
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