Canonical Allele Identifier: CA363565043

Gene: BTNL2 TSBP1-AS1

Linked Data

• dbSNP Id: rs1425505924
• MyVariant Identifiers: chr6:g.32363870G>C (hg19) ; chr6:g.32396093G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396093G>C , CM000668.2:g.32396093G>C	GRCh38
NC_000006.11:g.32363870G>C , CM000668.1:g.32363870G>C	GRCh37
NC_000006.10:g.32471848G>C	NCBI36
NG_054759.1:g.17787C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.452C>G (BTNL2)
ENST00000454136.8:c.1024C>G (BTNL2) MANE Select	ENSP00000390613.3:p.Leu342Val
ENST00000465865.6:c.*299C>G (BTNL2)	ENSP00000420063.1:n.*299C>G
ENST00000544175.3:c.*285C>G (BTNL2)	ENSP00000443364.2:n.*285C>G
ENST00000374993.4:c.1024C>G (BTNL2)	ENSP00000364132.1:p.Leu342Val
ENST00000454136.7:c.1024C>G (BTNL2)	ENSP00000390613.3:p.Leu342Val
ENST00000465865.5:c.506C>G (BTNL2)	ENSP00000420063.1:n.506C>G
ENST00000544175.2:c.193C>G (BTNL2)	ENSP00000443364.1:p.Leu65Val
NM_001304561.1:c.1024C>G (BTNL2)	NP_001291490.1:p.Leu342Val
XM_011514755.1:c.1024C>G (BTNL2)	XP_011513057.1:p.Leu342Val
XM_011514756.1:c.742C>G (BTNL2)	XP_011513058.1:p.Leu248Val
XM_011515039.1:c.482-9361G>C (TSBP1-AS1)	XP_011513341.1:n.482-9361G>C
NR_136245.1:n.303-9361G>C (TSBP1-AS1)
XM_017011057.1:c.1024C>G (BTNL2)	XP_016866546.1:p.Leu342Val
NM_001304561.2:c.1024C>G (BTNL2) MANE Select	NP_001291490.1:p.Leu342Val