Canonical Allele Identifier: CA480090790
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.54367472A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973688A>G , CM000674.2:g.53973688A>G GRCh38
NC_000012.11:g.54367472A>G , CM000674.1:g.54367472A>G GRCh37
NC_000012.10:g.52653739A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.447A>G (HOXC11) ENSP00000243082.4:p.Gln149=
ENST00000546378.1:c.447A>G (HOXC11) MANE Select ENSP00000446680.1:p.Gln149=
NM_014212.3:c.447A>G (HOXC11) NP_055027.1:p.Gln149=
NR_047517.1:n.59+1210T>C (HOTAIR)
NM_014212.4:c.447A>G (HOXC11) MANE Select NP_055027.1:p.Gln149=
Search 100 bp 5'
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