Canonical Allele Identifier: CA88166712

Gene: FNDC3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172208583T>A , CM000665.2:g.172208583T>A	GRCh38
NC_000003.11:g.171926373T>A , CM000665.1:g.171926373T>A	GRCh37
NC_000003.10:g.173409067T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415807.7:c.188-18288T>A MANE Select	ENSP00000411242.2:n.188-18288T>A
ENST00000336824.8:c.188-18288T>A	ENSP00000338523.4:n.188-18288T>A
ENST00000415807.6:c.188-18288T>A	ENSP00000411242.2:n.188-18288T>A
ENST00000416957.5:c.188-18288T>A	ENSP00000389094.1:n.188-18288T>A
ENST00000443501.1:c.107-18288T>A	ENSP00000389064.1:n.107-18288T>A
ENST00000469491.5:n.329-18288T>A
ENST00000478016.1:n.162-18288T>A
NM_001135095.1:c.188-18288T>A	NP_001128567.1:n.188-18288T>A
NM_022763.3:c.188-18288T>A	NP_073600.3:n.188-18288T>A
XM_011513083.1:c.107-18288T>A	XP_011511385.1:n.107-18288T>A
XM_011513084.1:c.107-18288T>A	XP_011511386.1:n.107-18288T>A
XM_017007062.1:c.188-18288T>A	XP_016862551.1:n.188-18288T>A
XM_017007064.2:c.188-18288T>A	XP_016862553.1:n.188-18288T>A
XM_024453716.1:c.188-18288T>A	XP_024309484.1:n.188-18288T>A
XM_024453717.1:c.188-18288T>A	XP_024309485.1:n.188-18288T>A
NM_022763.4:c.188-18288T>A MANE Select	NP_073600.3:n.188-18288T>A
NM_001135095.2:c.188-18288T>A	NP_001128567.1:n.188-18288T>A