Canonical Allele Identifier: CA1619538952

Gene: BTNL2 TSBP1-AS1

Linked Data

• dbSNP Id: rs1776421987

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32395990A>C , CM000668.2:g.32395990A>C	GRCh38
NC_000006.11:g.32363767A>C , CM000668.1:g.32363767A>C	GRCh37
NC_000006.10:g.32471745A>C	NCBI36
NG_054759.1:g.17890T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.506+49T>G (BTNL2)
ENST00000454136.8:c.1078+49T>G (BTNL2) MANE Select	ENSP00000390613.3:n.1078+49T>G
ENST00000465865.6:c.*349+53T>G (BTNL2)	ENSP00000420063.1:n.*349+53T>G
ENST00000544175.3:c.*339+49T>G (BTNL2)	ENSP00000443364.2:n.*339+49T>G
ENST00000374993.4:c.1078+49T>G (BTNL2)	ENSP00000364132.1:n.1078+49T>G
ENST00000454136.7:c.1078+49T>G (BTNL2)	ENSP00000390613.3:n.1078+49T>G
ENST00000465865.5:c.556+53T>G (BTNL2)	ENSP00000420063.1:n.556+53T>G
ENST00000544175.2:c.247+49T>G (BTNL2)	ENSP00000443364.1:n.247+49T>G
NM_001304561.1:c.1078+49T>G (BTNL2)	NP_001291490.1:n.1078+49T>G
XM_011514755.1:c.1074+53T>G (BTNL2)	XP_011513057.1:n.1074+53T>G
XM_011514756.1:c.*32T>G (BTNL2)	XP_011513058.1:n.*32T>G
XM_011515039.1:c.482-9464A>C (TSBP1-AS1)	XP_011513341.1:n.482-9464A>C
NR_136245.1:n.303-9464A>C (TSBP1-AS1)
XM_017011057.1:c.1078+49T>G (BTNL2)	XP_016866546.1:n.1078+49T>G
NM_001304561.2:c.1078+49T>G (BTNL2) MANE Select	NP_001291490.1:n.1078+49T>G