Canonical Allele Identifier: CA434970779

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112185018T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466171T>A , CM000665.2:g.112466171T>A	GRCh38
NC_000003.11:g.112185018T>A , CM000665.1:g.112185018T>A	GRCh37
NC_000003.10:g.113667708T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.807A>T MANE Select	ENSP00000333919.5:p.Ser269=
ENST00000334529.9:c.807A>T	ENSP00000333919.5:p.Ser269=
ENST00000383680.4:c.663A>T	ENSP00000373178.4:p.Ser221=
ENST00000474965.1:n.311A>T
NM_001085357.1:c.663A>T	NP_001078826.1:p.Ser221=
NM_181780.3:c.807A>T	NP_861445.3:p.Ser269=
XM_011512446.1:c.825A>T	XP_011510748.1:p.Ser275=
XM_011512447.1:c.825A>T	XP_011510749.1:p.Ser275=
XM_011512447.3:c.825A>T	XP_011510749.1:p.Ser275=
XM_017005748.2:c.807A>T	XP_016861237.1:p.Ser269=
NM_181780.4:c.807A>T MANE Select	NP_861445.4:p.Ser269=
NM_001085357.2:c.663A>T	NP_001078826.1:p.Ser221=