Canonical Allele Identifier: CA363564994

Gene: BTNL2 TSBP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.32363860T>C (hg19) ; chr6:g.32396083T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396083T>C , CM000668.2:g.32396083T>C	GRCh38
NC_000006.11:g.32363860T>C , CM000668.1:g.32363860T>C	GRCh37
NC_000006.10:g.32471838T>C	NCBI36
NG_054759.1:g.17797A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.462A>G (BTNL2)
ENST00000454136.8:c.1034A>G (BTNL2) MANE Select	ENSP00000390613.3:p.Lys345Arg
ENST00000465865.6:c.*309A>G (BTNL2)	ENSP00000420063.1:n.*309A>G
ENST00000544175.3:c.*295A>G (BTNL2)	ENSP00000443364.2:n.*295A>G
ENST00000374993.4:c.1034A>G (BTNL2)	ENSP00000364132.1:p.Lys345Arg
ENST00000454136.7:c.1034A>G (BTNL2)	ENSP00000390613.3:p.Lys345Arg
ENST00000465865.5:c.516A>G (BTNL2)	ENSP00000420063.1:n.516A>G
ENST00000544175.2:c.203A>G (BTNL2)	ENSP00000443364.1:p.Lys68Arg
NM_001304561.1:c.1034A>G (BTNL2)	NP_001291490.1:p.Lys345Arg
XM_011514755.1:c.1034A>G (BTNL2)	XP_011513057.1:p.Lys345Arg
XM_011514756.1:c.752A>G (BTNL2)	XP_011513058.1:p.Lys251Arg
XM_011515039.1:c.482-9371T>C (TSBP1-AS1)	XP_011513341.1:n.482-9371T>C
NR_136245.1:n.303-9371T>C (TSBP1-AS1)
XM_017011057.1:c.1034A>G (BTNL2)	XP_016866546.1:p.Lys345Arg
NM_001304561.2:c.1034A>G (BTNL2) MANE Select	NP_001291490.1:p.Lys345Arg