Canonical Allele Identifier: CA15506602

Gene: TBL2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73568544C>T , CM000669.2:g.73568544C>T	GRCh38
NC_000007.13:g.72982874C>T , CM000669.1:g.72982874C>T	GRCh37
NC_000007.12:g.72620810C>T	NCBI36
NG_023281.1:g.15140G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305632.11:c.*1963G>A MANE Select	ENSP00000307260.4:n.*1963G>A
NM_001362660.2:c.*1963G>A	NP_001349589.1:n.*1963G>A
NM_001362661.2:c.*1963G>A	NP_001349590.1:n.*1963G>A
NM_001362662.2:c.*1963G>A	NP_001349591.1:n.*1963G>A
NM_001362663.2:c.*1963G>A	NP_001349592.1:n.*1963G>A
NM_012453.4:c.*1963G>A MANE Select	NP_036585.1:n.*1963G>A