Canonical Allele Identifier: CA434970771

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112185009T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466162T>G , CM000665.2:g.112466162T>G	GRCh38
NC_000003.11:g.112185009T>G , CM000665.1:g.112185009T>G	GRCh37
NC_000003.10:g.113667699T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.816A>C MANE Select	ENSP00000333919.5:p.Ala272=
ENST00000334529.9:c.816A>C	ENSP00000333919.5:p.Ala272=
ENST00000383680.4:c.672A>C	ENSP00000373178.4:p.Ala224=
ENST00000474965.1:n.320A>C
NM_001085357.1:c.672A>C	NP_001078826.1:p.Ala224=
NM_181780.3:c.816A>C	NP_861445.3:p.Ala272=
XM_011512446.1:c.834A>C	XP_011510748.1:p.Ala278=
XM_011512447.1:c.834A>C	XP_011510749.1:p.Ala278=
XM_011512447.3:c.834A>C	XP_011510749.1:p.Ala278=
XM_017005748.2:c.816A>C	XP_016861237.1:p.Ala272=
NM_181780.4:c.816A>C MANE Select	NP_861445.4:p.Ala272=
NM_001085357.2:c.672A>C	NP_001078826.1:p.Ala224=