Canonical Allele Identifier: CA363564974

Gene: BTNL2 TSBP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.32363855C>G (hg19) ; chr6:g.32396078C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396078C>G , CM000668.2:g.32396078C>G	GRCh38
NC_000006.11:g.32363855C>G , CM000668.1:g.32363855C>G	GRCh37
NC_000006.10:g.32471833C>G	NCBI36
NG_054759.1:g.17802G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.467G>C (BTNL2)
ENST00000454136.8:c.1039G>C (BTNL2) MANE Select	ENSP00000390613.3:p.Asp347His
ENST00000465865.6:c.*314G>C (BTNL2)	ENSP00000420063.1:n.*314G>C
ENST00000544175.3:c.*300G>C (BTNL2)	ENSP00000443364.2:n.*300G>C
ENST00000374993.4:c.1039G>C (BTNL2)	ENSP00000364132.1:p.Asp347His
ENST00000454136.7:c.1039G>C (BTNL2)	ENSP00000390613.3:p.Asp347His
ENST00000465865.5:c.521G>C (BTNL2)	ENSP00000420063.1:n.521G>C
ENST00000544175.2:c.208G>C (BTNL2)	ENSP00000443364.1:p.Asp70His
NM_001304561.1:c.1039G>C (BTNL2)	NP_001291490.1:p.Asp347His
XM_011514755.1:c.1039G>C (BTNL2)	XP_011513057.1:p.Asp347His
XM_011514756.1:c.757G>C (BTNL2)	XP_011513058.1:p.Asp253His
XM_011515039.1:c.482-9376C>G (TSBP1-AS1)	XP_011513341.1:n.482-9376C>G
NR_136245.1:n.303-9376C>G (TSBP1-AS1)
XM_017011057.1:c.1039G>C (BTNL2)	XP_016866546.1:p.Asp347His
NM_001304561.2:c.1039G>C (BTNL2) MANE Select	NP_001291490.1:p.Asp347His