Canonical Allele Identifier: CA14927900

Gene: TNRC6B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40279087A>G , CM000684.2:g.40279087A>G	GRCh38
NC_000022.10:g.40675091A>G , CM000684.1:g.40675091A>G	GRCh37
NC_000022.9:g.39005037A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454349.7:c.3263-908A>G MANE Select	ENSP00000401946.2:n.3263-908A>G
ENST00000301923.13:c.1022-908A>G	ENSP00000306759.9:n.1022-908A>G
ENST00000335727.13:c.3104-908A>G	ENSP00000338371.8:n.3104-908A>G
ENST00000402203.5:c.1022-908A>G	ENSP00000384795.1:n.1022-908A>G
ENST00000446273.1:c.2491-908A>G
ENST00000454349.6:c.3263-908A>G	ENSP00000401946.2:n.3263-908A>G
ENST00000497559.1:n.264-908A>G
NM_001024843.1:c.1022-908A>G	NP_001020014.1:n.1022-908A>G
NM_001162501.1:c.3263-908A>G	NP_001155973.1:n.3263-908A>G
NM_015088.2:c.3104-908A>G	NP_055903.2:n.3104-908A>G
NM_001162501.2:c.3263-908A>G MANE Select	NP_001155973.1:n.3263-908A>G
NM_015088.3:c.3104-908A>G	NP_055903.2:n.3104-908A>G
NM_001024843.2:c.1022-908A>G	NP_001020014.1:n.1022-908A>G