Canonical Allele Identifier: CA258232754

Gene: MIR3171HG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.27330971C>T , CM000676.2:g.27330971C>T	GRCh38
NC_000014.8:g.27800177C>T , CM000676.1:g.27800177C>T	GRCh37
NC_000014.7:g.26870017C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553392.5:n.263-8830G>A
ENST00000554904.5:n.254-8830G>A
ENST00000555797.1:n.349-8830G>A
ENST00000556890.1:n.359-8830G>A
XR_110268.4:n.359-8830G>A
XR_943665.1:n.254-8830G>A
NR_148991.1:n.254-8830G>A
NR_148992.1:n.359-8830G>A