Canonical Allele Identifier: CA6604285
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs34745448
ExAC: 12:54367722 C / T
gnomAD v2: 12-54367722-C-T
gnomAD v3: 12-53973938-C-T
gnomAD v4: 12-53973938-C-T
MyVariant Identifiers: chr12:g.54367722C>T (hg19) chr12:g.53973938C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973938C>T , CM000674.2:g.53973938C>T GRCh38
NC_000012.11:g.54367722C>T , CM000674.1:g.54367722C>T GRCh37
NC_000012.10:g.52653989C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.686+11C>T (HOXC11) ENSP00000243082.4:n.686+11C>T
ENST00000546378.1:c.682+15C>T (HOXC11) MANE Select ENSP00000446680.1:n.682+15C>T
NM_014212.3:c.682+15C>T (HOXC11) NP_055027.1:n.682+15C>T
NR_047517.1:n.59+960G>A (HOTAIR)
NM_014212.4:c.682+15C>T (HOXC11) MANE Select NP_055027.1:n.682+15C>T
Search 100 bp 5'
Search 100 bp 3'