Canonical Allele Identifier: CA434970784

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112185024C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466177C>G , CM000665.2:g.112466177C>G	GRCh38
NC_000003.11:g.112185024C>G , CM000665.1:g.112185024C>G	GRCh37
NC_000003.10:g.113667714C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.801G>C MANE Select	ENSP00000333919.5:p.Pro267=
ENST00000334529.9:c.801G>C	ENSP00000333919.5:p.Pro267=
ENST00000383680.4:c.657G>C	ENSP00000373178.4:p.Pro219=
ENST00000474965.1:n.305G>C
NM_001085357.1:c.657G>C	NP_001078826.1:p.Pro219=
NM_181780.3:c.801G>C	NP_861445.3:p.Pro267=
XM_011512446.1:c.819G>C	XP_011510748.1:p.Pro273=
XM_011512447.1:c.819G>C	XP_011510749.1:p.Pro273=
XM_011512447.3:c.819G>C	XP_011510749.1:p.Pro273=
XM_017005748.2:c.801G>C	XP_016861237.1:p.Pro267=
NM_181780.4:c.801G>C MANE Select	NP_861445.4:p.Pro267=
NM_001085357.2:c.657G>C	NP_001078826.1:p.Pro219=