Canonical Allele Identifier: CA2405673513

Gene: TNRC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40256869A= , CM000684.2:g.40256869A=	GRCh38
NC_000022.10:g.40652873A= , CM000684.1:g.40652873A=	GRCh37
NC_000022.9:g.38982819A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001162501.2:c.116-4963A= MANE Select	NP_001155973.1:n.116-4963A=
ENST00000454349.7:c.116-4963A= MANE Select	ENSP00000401946.2:n.116-4963A=
NM_001024843.1:c.224-4963A=	NP_001020014.1:n.224-4963A=
NM_001024843.2:c.224-4963A=	NP_001020014.1:n.224-4963A=
NM_001162501.1:c.116-4963A=	NP_001155973.1:n.116-4963A=
NM_015088.2:c.116-4963A=	NP_055903.2:n.116-4963A=
NM_015088.3:c.116-4963A=	NP_055903.2:n.116-4963A=
ENST00000301923.13:c.224-4963A=	ENSP00000306759.9:n.224-4963A=
ENST00000335727.13:c.116-4963A=	ENSP00000338371.8:n.116-4963A=
ENST00000402203.5:c.224-4963A=	ENSP00000384795.1:n.224-4963A=
ENST00000454349.6:c.116-4963A=	ENSP00000401946.2:n.116-4963A=