Canonical Allele Identifier: CA363564947

Gene: BTNL2 TSBP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.32363845T>A (hg19) ; chr6:g.32396068T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396068T>A , CM000668.2:g.32396068T>A	GRCh38
NC_000006.11:g.32363845T>A , CM000668.1:g.32363845T>A	GRCh37
NC_000006.10:g.32471823T>A	NCBI36
NG_054759.1:g.17812A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374993.5:n.477A>T (BTNL2)
ENST00000454136.8:c.1049A>T (BTNL2) MANE Select	ENSP00000390613.3:p.Gln350Leu
ENST00000465865.6:c.*324A>T (BTNL2)	ENSP00000420063.1:n.*324A>T
ENST00000544175.3:c.*310A>T (BTNL2)	ENSP00000443364.2:n.*310A>T
ENST00000374993.4:c.1049A>T (BTNL2)	ENSP00000364132.1:p.Gln350Leu
ENST00000454136.7:c.1049A>T (BTNL2)	ENSP00000390613.3:p.Gln350Leu
ENST00000465865.5:c.531A>T (BTNL2)	ENSP00000420063.1:n.531A>T
ENST00000544175.2:c.218A>T (BTNL2)	ENSP00000443364.1:p.Gln73Leu
NM_001304561.1:c.1049A>T (BTNL2)	NP_001291490.1:p.Gln350Leu
XM_011514755.1:c.1049A>T (BTNL2)	XP_011513057.1:p.Gln350Leu
XM_011514756.1:c.767A>T (BTNL2)	XP_011513058.1:p.Gln256Leu
XM_011515039.1:c.482-9386T>A (TSBP1-AS1)	XP_011513341.1:n.482-9386T>A
NR_136245.1:n.303-9386T>A (TSBP1-AS1)
XM_017011057.1:c.1049A>T (BTNL2)	XP_016866546.1:p.Gln350Leu
NM_001304561.2:c.1049A>T (BTNL2) MANE Select	NP_001291490.1:p.Gln350Leu