Canonical Allele Identifier: CA823999573

Gene: BTNL2 TSBP1-AS1

Linked Data

• dbSNP Id: rs1351641148
• gnomAD v3: 6-32405437-A-G
• gnomAD v4: 6-32405437-A-G
• MyVariant Identifiers: chr6:g.32373214A>G (hg19) ; chr6:g.32405437A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32405437A>G , CM000668.2:g.32405437A>G	GRCh38
NC_000006.11:g.32373214A>G , CM000668.1:g.32373214A>G	GRCh37
NC_000006.10:g.32481192A>G	NCBI36
NG_054759.1:g.8443T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374993.5:n.137+1608T>C (BTNL2)
ENST00000446536.3:c.80-154T>C (BTNL2)	ENSP00000388434.2:n.80-154T>C
ENST00000454136.8:c.80-151T>C (BTNL2) MANE Select	ENSP00000390613.3:n.80-151T>C
ENST00000465865.6:c.80-151T>C (BTNL2)	ENSP00000420063.1:n.80-151T>C
ENST00000544175.3:c.80-151T>C (BTNL2)	ENSP00000443364.2:n.80-151T>C
ENST00000374993.4:c.80-151T>C (BTNL2)	ENSP00000364132.1:n.80-151T>C
ENST00000446536.2:c.80-154T>C (BTNL2)	ENSP00000388434.2:n.80-154T>C
ENST00000454136.7:c.80-151T>C (BTNL2)	ENSP00000390613.3:n.80-151T>C
ENST00000465865.5:c.80-151T>C (BTNL2)	ENSP00000420063.1:n.80-151T>C
ENST00000544175.2:c.-229-151T>C (BTNL2)	ENSP00000443364.1:n.-229-151T>C
NM_001304561.1:c.80-151T>C (BTNL2)	NP_001291490.1:n.80-151T>C
XM_011514755.1:c.80-151T>C (BTNL2)	XP_011513057.1:n.80-151T>C
XM_011514756.1:c.80-151T>C (BTNL2)	XP_011513058.1:n.80-151T>C
XM_011515039.1:c.482-17A>G (TSBP1-AS1)	XP_011513341.1:n.482-17A>G
XR_926699.1:n.104-17A>G (TSBP1-AS1)
NR_136245.1:n.303-17A>G (TSBP1-AS1)
XM_017011057.1:c.80-151T>C (BTNL2)	XP_016866546.1:n.80-151T>C
NM_001304561.2:c.80-151T>C (BTNL2) MANE Select	NP_001291490.1:n.80-151T>C