Canonical Allele Identifier: CA363564960

Gene: BTNL2 TSBP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.32363851A>G (hg19) ; chr6:g.32396074A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396074A>G , CM000668.2:g.32396074A>G	GRCh38
NC_000006.11:g.32363851A>G , CM000668.1:g.32363851A>G	GRCh37
NC_000006.10:g.32471829A>G	NCBI36
NG_054759.1:g.17806T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.471T>C (BTNL2)
ENST00000454136.8:c.1043T>C (BTNL2) MANE Select	ENSP00000390613.3:p.Val348Ala
ENST00000465865.6:c.*318T>C (BTNL2)	ENSP00000420063.1:n.*318T>C
ENST00000544175.3:c.*304T>C (BTNL2)	ENSP00000443364.2:n.*304T>C
ENST00000374993.4:c.1043T>C (BTNL2)	ENSP00000364132.1:p.Val348Ala
ENST00000454136.7:c.1043T>C (BTNL2)	ENSP00000390613.3:p.Val348Ala
ENST00000465865.5:c.525T>C (BTNL2)	ENSP00000420063.1:n.525T>C
ENST00000544175.2:c.212T>C (BTNL2)	ENSP00000443364.1:p.Val71Ala
NM_001304561.1:c.1043T>C (BTNL2)	NP_001291490.1:p.Val348Ala
XM_011514755.1:c.1043T>C (BTNL2)	XP_011513057.1:p.Val348Ala
XM_011514756.1:c.761T>C (BTNL2)	XP_011513058.1:p.Val254Ala
XM_011515039.1:c.482-9380A>G (TSBP1-AS1)	XP_011513341.1:n.482-9380A>G
NR_136245.1:n.303-9380A>G (TSBP1-AS1)
XM_017011057.1:c.1043T>C (BTNL2)	XP_016866546.1:p.Val348Ala
NM_001304561.2:c.1043T>C (BTNL2) MANE Select	NP_001291490.1:p.Val348Ala