Canonical Allele Identifier: CA1619546093
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32405452A= , CM000668.2:g.32405452A= GRCh38
NC_000006.11:g.32373229A= , CM000668.1:g.32373229A= GRCh37
NC_000006.10:g.32481207A= NCBI36
NG_054759.1:g.8428T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374993.5:n.137+1593T= (BTNL2)
ENST00000446536.3:c.80-169T= (BTNL2) ENSP00000388434.2:n.80-169T=
ENST00000454136.8:c.80-166T= (BTNL2) MANE Select ENSP00000390613.3:n.80-166T=
ENST00000465865.6:c.80-166T= (BTNL2) ENSP00000420063.1:n.80-166T=
ENST00000544175.3:c.80-166T= (BTNL2) ENSP00000443364.2:n.80-166T=
ENST00000374993.4:c.80-166T= (BTNL2) ENSP00000364132.1:n.80-166T=
ENST00000446536.2:c.80-169T= (BTNL2) ENSP00000388434.2:n.80-169T=
ENST00000454136.7:c.80-166T= (BTNL2) ENSP00000390613.3:n.80-166T=
ENST00000465865.5:c.80-166T= (BTNL2) ENSP00000420063.1:n.80-166T=
ENST00000544175.2:c.-229-166T= (BTNL2) ENSP00000443364.1:n.-229-166T=
NM_001304561.1:c.80-166T= (BTNL2) NP_001291490.1:n.80-166T=
XM_011514755.1:c.80-166T= (BTNL2) XP_011513057.1:n.80-166T=
XM_011514756.1:c.80-166T= (BTNL2) XP_011513058.1:n.80-166T=
XM_011515039.1:c.482-2A= (TSBP1-AS1) XP_011513341.1:n.482-2A=
XR_926699.1:n.104-2A= (TSBP1-AS1)
NR_136245.1:n.303-2A= (TSBP1-AS1)
XM_017011057.1:c.80-166T= (BTNL2) XP_016866546.1:n.80-166T=
NM_001304561.2:c.80-166T= (BTNL2) MANE Select NP_001291490.1:n.80-166T=