Canonical Allele Identifier: CA15435071

Gene: BTNL2 TSBP1-AS1

Linked Data

• dbSNP Id: rs2076533
• gnomAD v2: 6-32363527-C-T
• gnomAD v3: 6-32395750-C-T
• gnomAD v4: 6-32395750-C-T
• MyVariant Identifiers: chr6:g.32363527C>T (hg19) ; chr6:g.32395750C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32395750C>T , CM000668.2:g.32395750C>T	GRCh38
NC_000006.11:g.32363527C>T , CM000668.1:g.32363527C>T	GRCh37
NC_000006.10:g.32471505C>T	NCBI36
NG_054759.1:g.18130G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374993.5:n.506+289G>A (BTNL2)
ENST00000454136.8:c.1078+289G>A (BTNL2) MANE Select	ENSP00000390613.3:n.1078+289G>A
ENST00000465865.6:c.*349+293G>A (BTNL2)	ENSP00000420063.1:n.*349+293G>A
ENST00000544175.3:c.*339+289G>A (BTNL2)	ENSP00000443364.2:n.*339+289G>A
ENST00000374993.4:c.1078+289G>A (BTNL2)	ENSP00000364132.1:n.1078+289G>A
ENST00000454136.7:c.1078+289G>A (BTNL2)	ENSP00000390613.3:n.1078+289G>A
ENST00000465865.5:c.556+293G>A (BTNL2)	ENSP00000420063.1:n.556+293G>A
ENST00000544175.2:c.247+289G>A (BTNL2)	ENSP00000443364.1:n.247+289G>A
NM_001304561.1:c.1078+289G>A (BTNL2)	NP_001291490.1:n.1078+289G>A
XM_011514755.1:c.1074+293G>A (BTNL2)	XP_011513057.1:n.1074+293G>A
XM_011514756.1:c.*272G>A (BTNL2)	XP_011513058.1:n.*272G>A
XM_011515039.1:c.482-9704C>T (TSBP1-AS1)	XP_011513341.1:n.482-9704C>T
NR_136245.1:n.303-9704C>T (TSBP1-AS1)
XM_017011057.1:c.1078+289G>A (BTNL2)	XP_016866546.1:n.1078+289G>A
NM_001304561.2:c.1078+289G>A (BTNL2) MANE Select	NP_001291490.1:n.1078+289G>A