Canonical Allele Identifier: CA353802341

Gene: BTLA

Linked Data

• dbSNP Id: rs2931761
• MyVariant Identifiers: chr3:g.112190137G>C (hg19) ; chr3:g.112471290G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112471290G>C , CM000665.2:g.112471290G>C	GRCh38
NC_000003.11:g.112190137G>C , CM000665.1:g.112190137G>C	GRCh37
NC_000003.10:g.113672827G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000334529.10:c.469C>G MANE Select	ENSP00000333919.5:p.Arg157Gly
ENST00000334529.9:c.469C>G	ENSP00000333919.5:p.Arg157Gly
ENST00000383680.4:c.404-1486C>G	ENSP00000373178.4:n.404-1486C>G
NM_001085357.1:c.404-1486C>G	NP_001078826.1:n.404-1486C>G
XM_011512446.1:c.487C>G	XP_011510748.1:p.Arg163Gly
XM_011512447.1:c.487C>G	XP_011510749.1:p.Arg163Gly
XM_011512447.3:c.487C>G	XP_011510749.1:p.Arg163Gly
XM_017005748.2:c.469C>G	XP_016861237.1:p.Arg157Gly
NM_181780.4:c.469C>G MANE Select	NP_861445.4:p.Arg157Gly
NM_001085357.2:c.404-1486C>G	NP_001078826.1:n.404-1486C>G