Canonical Allele Identifier: CA566377404
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1163199302
gnomAD v2: 6-32369425-A-G
gnomAD v3: 6-32401648-A-G
gnomAD v4: 6-32401648-A-G
MyVariant Identifiers: chr6:g.32369425A>G (hg19) chr6:g.32401648A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32401648A>G , CM000668.2:g.32401648A>G GRCh38
NC_000006.11:g.32369425A>G , CM000668.1:g.32369425A>G GRCh37
NC_000006.10:g.32477403A>G NCBI36
NG_054759.1:g.12232T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374993.5:n.158+137T>C (BTNL2)
ENST00000454136.8:c.730+137T>C (BTNL2) MANE Select ENSP00000390613.3:n.730+137T>C
ENST00000465865.6:c.*5+137T>C (BTNL2) ENSP00000420063.1:n.*5+137T>C
ENST00000544175.3:c.207+137T>C (BTNL2) ENSP00000443364.2:n.207+137T>C
ENST00000374993.4:c.730+137T>C (BTNL2) ENSP00000364132.1:n.730+137T>C
ENST00000454136.7:c.730+137T>C (BTNL2) ENSP00000390613.3:n.730+137T>C
ENST00000465865.5:c.212+137T>C (BTNL2) ENSP00000420063.1:n.212+137T>C
ENST00000544175.2:c.-102+137T>C (BTNL2) ENSP00000443364.1:n.-102+137T>C
NM_001304561.1:c.730+137T>C (BTNL2) NP_001291490.1:n.730+137T>C
XM_011514755.1:c.730+137T>C (BTNL2) XP_011513057.1:n.730+137T>C
XM_011514756.1:c.448+137T>C (BTNL2) XP_011513058.1:n.448+137T>C
XM_011515039.1:c.482-3806A>G (TSBP1-AS1) XP_011513341.1:n.482-3806A>G
NR_136245.1:n.303-3806A>G (TSBP1-AS1)
XM_017011057.1:c.730+137T>C (BTNL2) XP_016866546.1:n.730+137T>C
NM_001304561.2:c.730+137T>C (BTNL2) MANE Select NP_001291490.1:n.730+137T>C
Search 100 bp 5'
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