Canonical Allele Identifier: CA363566154
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32403058T>A , CM000668.2:g.32403058T>A GRCh38
NC_000006.11:g.32370835T>A , CM000668.1:g.32370835T>A GRCh37
NC_000006.10:g.32478813T>A NCBI36
NG_054759.1:g.10822A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374993.5:n.138-1253A>T (BTNL2)
ENST00000454136.8:c.586A>T (BTNL2) MANE Select ENSP00000390613.3:p.Lys196Ter
ENST00000465865.6:c.192-1253A>T (BTNL2) ENSP00000420063.1:n.192-1253A>T
ENST00000544175.3:c.187-1253A>T (BTNL2) ENSP00000443364.2:n.187-1253A>T
ENST00000374993.4:c.586A>T (BTNL2) ENSP00000364132.1:p.Lys196Ter
ENST00000454136.7:c.586A>T (BTNL2) ENSP00000390613.3:p.Lys196Ter
ENST00000465865.5:c.192-1253A>T (BTNL2) ENSP00000420063.1:n.192-1253A>T
ENST00000544175.2:c.-122-1253A>T (BTNL2) ENSP00000443364.1:n.-122-1253A>T
NM_001304561.1:c.586A>T (BTNL2) NP_001291490.1:p.Lys196Ter
XM_011514755.1:c.586A>T (BTNL2) XP_011513057.1:p.Lys196Ter
XM_011514756.1:c.428-1253A>T (BTNL2) XP_011513058.1:n.428-1253A>T
XM_011515039.1:c.482-2396T>A (TSBP1-AS1) XP_011513341.1:n.482-2396T>A
NR_136245.1:n.303-2396T>A (TSBP1-AS1)
XM_017011057.1:c.586A>T (BTNL2) XP_016866546.1:p.Lys196Ter
NM_001304561.2:c.586A>T (BTNL2) MANE Select NP_001291490.1:p.Lys196Ter
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