Canonical Allele Identifier: CA902654923

Gene: FNDC3B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172277815C>A , CM000665.2:g.172277815C>A	GRCh38
NC_000003.11:g.171995605C>A , CM000665.1:g.171995605C>A	GRCh37
NC_000003.10:g.173478299C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_022763.4:c.791-8111C>A MANE Select	NP_073600.3:n.791-8111C>A
ENST00000415807.7:c.791-8111C>A MANE Select	ENSP00000411242.2:n.791-8111C>A
NM_001135095.1:c.791-8111C>A	NP_001128567.1:n.791-8111C>A
NM_001135095.2:c.791-8111C>A	NP_001128567.1:n.791-8111C>A
NM_022763.3:c.791-8111C>A	NP_073600.3:n.791-8111C>A
ENST00000336824.8:c.791-8111C>A	ENSP00000338523.4:n.791-8111C>A
ENST00000415807.6:c.791-8111C>A	ENSP00000411242.2:n.791-8111C>A
ENST00000416957.5:c.791-8111C>A	ENSP00000389094.1:n.791-8111C>A
ENST00000469491.5:n.932-8111C>A
XM_011513083.1:c.710-8111C>A	XP_011511385.1:n.710-8111C>A
XM_011513084.1:c.428-8111C>A	XP_011511386.1:n.428-8111C>A
XM_017007062.1:c.509-8111C>A	XP_016862551.1:n.509-8111C>A
XM_017007063.1:c.47-8111C>A	XP_016862552.1:n.47-8111C>A
XM_017007064.2:c.791-8111C>A	XP_016862553.1:n.791-8111C>A
XM_024453716.1:c.791-8111C>A	XP_024309484.1:n.791-8111C>A
XM_024453717.1:c.791-8111C>A	XP_024309485.1:n.791-8111C>A