Canonical Allele Identifier: CA363565009

Gene: BTNL2 TSBP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.32363862T>G (hg19) ; chr6:g.32396085T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396085T>G , CM000668.2:g.32396085T>G	GRCh38
NC_000006.11:g.32363862T>G , CM000668.1:g.32363862T>G	GRCh37
NC_000006.10:g.32471840T>G	NCBI36
NG_054759.1:g.17795A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374993.5:n.460A>C (BTNL2)
ENST00000454136.8:c.1032A>C (BTNL2) MANE Select	ENSP00000390613.3:p.Glu344Asp
ENST00000465865.6:c.*307A>C (BTNL2)	ENSP00000420063.1:n.*307A>C
ENST00000544175.3:c.*293A>C (BTNL2)	ENSP00000443364.2:n.*293A>C
ENST00000374993.4:c.1032A>C (BTNL2)	ENSP00000364132.1:p.Glu344Asp
ENST00000454136.7:c.1032A>C (BTNL2)	ENSP00000390613.3:p.Glu344Asp
ENST00000465865.5:c.514A>C (BTNL2)	ENSP00000420063.1:n.514A>C
ENST00000544175.2:c.201A>C (BTNL2)	ENSP00000443364.1:p.Glu67Asp
NM_001304561.1:c.1032A>C (BTNL2)	NP_001291490.1:p.Glu344Asp
XM_011514755.1:c.1032A>C (BTNL2)	XP_011513057.1:p.Glu344Asp
XM_011514756.1:c.750A>C (BTNL2)	XP_011513058.1:p.Glu250Asp
XM_011515039.1:c.482-9369T>G (TSBP1-AS1)	XP_011513341.1:n.482-9369T>G
NR_136245.1:n.303-9369T>G (TSBP1-AS1)
XM_017011057.1:c.1032A>C (BTNL2)	XP_016866546.1:p.Glu344Asp
NM_001304561.2:c.1032A>C (BTNL2) MANE Select	NP_001291490.1:p.Glu344Asp