Canonical Allele Identifier: CA411637815

Gene: TNRC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40266871C>T , CM000684.2:g.40266871C>T	GRCh38
NC_000022.10:g.40662875C>T , CM000684.1:g.40662875C>T	GRCh37
NC_000022.9:g.38992821C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001162501.2:c.2641C>T MANE Select	NP_001155973.1:p.Gln881Ter
ENST00000454349.7:c.2641C>T MANE Select	ENSP00000401946.2:p.Gln881Ter
NM_001024843.1:c.566-3251C>T	NP_001020014.1:n.566-3251C>T
NM_001024843.2:c.566-3251C>T	NP_001020014.1:n.566-3251C>T
NM_001162501.1:c.2641C>T	NP_001155973.1:p.Gln881Ter
NM_015088.2:c.2641C>T	NP_055903.2:p.Gln881Ter
NM_015088.3:c.2641C>T	NP_055903.2:p.Gln881Ter
ENST00000301923.13:c.566-3251C>T	ENSP00000306759.9:n.566-3251C>T
ENST00000335727.13:c.2641C>T	ENSP00000338371.8:p.Gln881Ter
ENST00000402203.5:c.566-3251C>T	ENSP00000384795.1:n.566-3251C>T
ENST00000446273.1:c.1869C>T
ENST00000454349.6:c.2641C>T	ENSP00000401946.2:p.Gln881Ter
XR_938265.1:n.318-6503G>A