Canonical Allele Identifier: CA3741286

Gene: BTNL2 TSBP1-AS1

Linked Data

• dbSNP Id: rs761761520
• ExAC: 6:32363857 T / A
• gnomAD v2: 6-32363857-T-A
• gnomAD v4: 6-32396080-T-A
• MyVariant Identifiers: chr6:g.32363857T>A (hg19) ; chr6:g.32396080T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396080T>A , CM000668.2:g.32396080T>A	GRCh38
NC_000006.11:g.32363857T>A , CM000668.1:g.32363857T>A	GRCh37
NC_000006.10:g.32471835T>A	NCBI36
NG_054759.1:g.17800A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.465A>T (BTNL2)
ENST00000454136.8:c.1037A>T (BTNL2) MANE Select	ENSP00000390613.3:p.Asp346Val
ENST00000465865.6:c.*312A>T (BTNL2)	ENSP00000420063.1:n.*312A>T
ENST00000544175.3:c.*298A>T (BTNL2)	ENSP00000443364.2:n.*298A>T
ENST00000374993.4:c.1037A>T (BTNL2)	ENSP00000364132.1:p.Asp346Val
ENST00000454136.7:c.1037A>T (BTNL2)	ENSP00000390613.3:p.Asp346Val
ENST00000465865.5:c.519A>T (BTNL2)	ENSP00000420063.1:n.519A>T
ENST00000544175.2:c.206A>T (BTNL2)	ENSP00000443364.1:p.Asp69Val
NM_001304561.1:c.1037A>T (BTNL2)	NP_001291490.1:p.Asp346Val
XM_011514755.1:c.1037A>T (BTNL2)	XP_011513057.1:p.Asp346Val
XM_011514756.1:c.755A>T (BTNL2)	XP_011513058.1:p.Asp252Val
XM_011515039.1:c.482-9374T>A (TSBP1-AS1)	XP_011513341.1:n.482-9374T>A
NR_136245.1:n.303-9374T>A (TSBP1-AS1)
XM_017011057.1:c.1037A>T (BTNL2)	XP_016866546.1:p.Asp346Val
NM_001304561.2:c.1037A>T (BTNL2) MANE Select	NP_001291490.1:p.Asp346Val