Canonical Allele Identifier: CA2578578325

Gene: BTNL2 TSBP1-AS1

Linked Data

• gnomAD v4: 6-32395988-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32395988A>T , CM000668.2:g.32395988A>T	GRCh38
NC_000006.11:g.32363765A>T , CM000668.1:g.32363765A>T	GRCh37
NC_000006.10:g.32471743A>T	NCBI36
NG_054759.1:g.17892T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.506+51T>A (BTNL2)
ENST00000454136.8:c.1078+51T>A (BTNL2) MANE Select	ENSP00000390613.3:n.1078+51T>A
ENST00000465865.6:c.*349+55T>A (BTNL2)	ENSP00000420063.1:n.*349+55T>A
ENST00000544175.3:c.*339+51T>A (BTNL2)	ENSP00000443364.2:n.*339+51T>A
ENST00000374993.4:c.1078+51T>A (BTNL2)	ENSP00000364132.1:n.1078+51T>A
ENST00000454136.7:c.1078+51T>A (BTNL2)	ENSP00000390613.3:n.1078+51T>A
ENST00000465865.5:c.556+55T>A (BTNL2)	ENSP00000420063.1:n.556+55T>A
ENST00000544175.2:c.247+51T>A (BTNL2)	ENSP00000443364.1:n.247+51T>A
NM_001304561.1:c.1078+51T>A (BTNL2)	NP_001291490.1:n.1078+51T>A
XM_011514755.1:c.1074+55T>A (BTNL2)	XP_011513057.1:n.1074+55T>A
XM_011514756.1:c.*34T>A (BTNL2)	XP_011513058.1:n.*34T>A
XM_011515039.1:c.482-9466A>T (TSBP1-AS1)	XP_011513341.1:n.482-9466A>T
NR_136245.1:n.303-9466A>T (TSBP1-AS1)
XM_017011057.1:c.1078+51T>A (BTNL2)	XP_016866546.1:n.1078+51T>A
NM_001304561.2:c.1078+51T>A (BTNL2) MANE Select	NP_001291490.1:n.1078+51T>A