Canonical Allele Identifier: CA15993949
Gene: TNRC6B HGNC NCBI

Linked Data

dbSNP Id: rs139909

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.40301577C>T , CM000684.2:g.40301577C>T GRCh38
NC_000022.10:g.40697581C>T , CM000684.1:g.40697581C>T GRCh37
NC_000022.9:g.39027527C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454349.7:c.4120+244C>T MANE Select ENSP00000401946.2:n.4120+244C>T
ENST00000301923.13:c.1708+244C>T ENSP00000306759.9:n.1708+244C>T
ENST00000335727.13:c.3790+244C>T ENSP00000338371.8:n.3790+244C>T
ENST00000402203.5:c.1708+244C>T ENSP00000384795.1:n.1708+244C>T
ENST00000446273.1:c.3177+244C>T
ENST00000454349.6:c.4120+244C>T ENSP00000401946.2:n.4120+244C>T
NM_001024843.1:c.1708+244C>T NP_001020014.1:n.1708+244C>T
NM_001162501.1:c.4120+244C>T NP_001155973.1:n.4120+244C>T
NM_015088.2:c.3790+244C>T NP_055903.2:n.3790+244C>T
NM_001162501.2:c.4120+244C>T MANE Select NP_001155973.1:n.4120+244C>T
NM_015088.3:c.3790+244C>T NP_055903.2:n.3790+244C>T
NM_001024843.2:c.1708+244C>T NP_001020014.1:n.1708+244C>T