Canonical Allele Identifier: CA363565034

Gene: BTNL2 TSBP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.32363867A>T (hg19) ; chr6:g.32396090A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396090A>T , CM000668.2:g.32396090A>T	GRCh38
NC_000006.11:g.32363867A>T , CM000668.1:g.32363867A>T	GRCh37
NC_000006.10:g.32471845A>T	NCBI36
NG_054759.1:g.17790T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.455T>A (BTNL2)
ENST00000454136.8:c.1027T>A (BTNL2) MANE Select	ENSP00000390613.3:p.Phe343Ile
ENST00000465865.6:c.*302T>A (BTNL2)	ENSP00000420063.1:n.*302T>A
ENST00000544175.3:c.*288T>A (BTNL2)	ENSP00000443364.2:n.*288T>A
ENST00000374993.4:c.1027T>A (BTNL2)	ENSP00000364132.1:p.Phe343Ile
ENST00000454136.7:c.1027T>A (BTNL2)	ENSP00000390613.3:p.Phe343Ile
ENST00000465865.5:c.509T>A (BTNL2)	ENSP00000420063.1:n.509T>A
ENST00000544175.2:c.196T>A (BTNL2)	ENSP00000443364.1:p.Phe66Ile
NM_001304561.1:c.1027T>A (BTNL2)	NP_001291490.1:p.Phe343Ile
XM_011514755.1:c.1027T>A (BTNL2)	XP_011513057.1:p.Phe343Ile
XM_011514756.1:c.745T>A (BTNL2)	XP_011513058.1:p.Phe249Ile
XM_011515039.1:c.482-9364A>T (TSBP1-AS1)	XP_011513341.1:n.482-9364A>T
NR_136245.1:n.303-9364A>T (TSBP1-AS1)
XM_017011057.1:c.1027T>A (BTNL2)	XP_016866546.1:p.Phe343Ile
NM_001304561.2:c.1027T>A (BTNL2) MANE Select	NP_001291490.1:p.Phe343Ile