Canonical Allele Identifier: CA12421107
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs10947261
gnomAD v2: 6-32373232-G-T
gnomAD v3: 6-32405455-G-T
gnomAD v4: 6-32405455-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32405455G>T , CM000668.2:g.32405455G>T GRCh38
NC_000006.11:g.32373232G>T , CM000668.1:g.32373232G>T GRCh37
NC_000006.10:g.32481210G>T NCBI36
NG_054759.1:g.8425C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374993.5:n.137+1590C>A (BTNL2)
ENST00000446536.3:c.80-172C>A (BTNL2) ENSP00000388434.2:n.80-172C>A
ENST00000454136.8:c.80-169C>A (BTNL2) MANE Select ENSP00000390613.3:n.80-169C>A
ENST00000465865.6:c.80-169C>A (BTNL2) ENSP00000420063.1:n.80-169C>A
ENST00000544175.3:c.80-169C>A (BTNL2) ENSP00000443364.2:n.80-169C>A
ENST00000374993.4:c.80-169C>A (BTNL2) ENSP00000364132.1:n.80-169C>A
ENST00000446536.2:c.80-172C>A (BTNL2) ENSP00000388434.2:n.80-172C>A
ENST00000454136.7:c.80-169C>A (BTNL2) ENSP00000390613.3:n.80-169C>A
ENST00000465865.5:c.80-169C>A (BTNL2) ENSP00000420063.1:n.80-169C>A
ENST00000544175.2:c.-229-169C>A (BTNL2) ENSP00000443364.1:n.-229-169C>A
NM_001304561.1:c.80-169C>A (BTNL2) NP_001291490.1:n.80-169C>A
XM_011514755.1:c.80-169C>A (BTNL2) XP_011513057.1:n.80-169C>A
XM_011514756.1:c.80-169C>A (BTNL2) XP_011513058.1:n.80-169C>A
XM_011515039.1:c.483G>T (TSBP1-AS1) XP_011513341.1:p.Glu161Asp
XR_926699.1:n.105G>T (TSBP1-AS1)
NR_136245.1:n.304G>T (TSBP1-AS1)
XM_017011057.1:c.80-169C>A (BTNL2) XP_016866546.1:n.80-169C>A
NM_001304561.2:c.80-169C>A (BTNL2) MANE Select NP_001291490.1:n.80-169C>A