Canonical Allele Identifier: CA2666960691

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466094-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466094A>C , CM000665.2:g.112466094A>C	GRCh38
NC_000003.11:g.112184941A>C , CM000665.1:g.112184941A>C	GRCh37
NC_000003.10:g.113667631A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.*14T>G MANE Select	ENSP00000333919.5:n.*14T>G
ENST00000334529.9:c.*14T>G	ENSP00000333919.5:n.*14T>G
ENST00000474965.1:n.388T>G
NM_001085357.1:c.*14T>G	NP_001078826.1:n.*14T>G
NM_181780.3:c.*14T>G	NP_861445.3:n.*14T>G
XM_011512446.1:c.*14T>G	XP_011510748.1:n.*14T>G
XM_011512447.1:c.*14T>G	XP_011510749.1:n.*14T>G
XM_011512447.3:c.*14T>G	XP_011510749.1:n.*14T>G
XM_017005748.2:c.*14T>G	XP_016861237.1:n.*14T>G
NM_181780.4:c.*14T>G MANE Select	NP_861445.4:n.*14T>G
NM_001085357.2:c.*14T>G	NP_001078826.1:n.*14T>G