Canonical Allele Identifier: CA479965457
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.54367664A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973880A>C , CM000674.2:g.53973880A>C GRCh38
NC_000012.11:g.54367664A>C , CM000674.1:g.54367664A>C GRCh37
NC_000012.10:g.52653931A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.639A>C (HOXC11) ENSP00000243082.4:p.Ser213=
ENST00000546378.1:c.639A>C (HOXC11) MANE Select ENSP00000446680.1:p.Ser213=
NM_014212.3:c.639A>C (HOXC11) NP_055027.1:p.Ser213=
NR_047517.1:n.59+1018T>G (HOTAIR)
NM_014212.4:c.639A>C (HOXC11) MANE Select NP_055027.1:p.Ser213=
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