Canonical Allele Identifier: CA2666960694

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466097-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466097C>A , CM000665.2:g.112466097C>A	GRCh38
NC_000003.11:g.112184944C>A , CM000665.1:g.112184944C>A	GRCh37
NC_000003.10:g.113667634C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.*11G>T MANE Select	ENSP00000333919.5:n.*11G>T
ENST00000334529.9:c.*11G>T	ENSP00000333919.5:n.*11G>T
ENST00000474965.1:n.385G>T
NM_001085357.1:c.*11G>T	NP_001078826.1:n.*11G>T
NM_181780.3:c.*11G>T	NP_861445.3:n.*11G>T
XM_011512446.1:c.*11G>T	XP_011510748.1:n.*11G>T
XM_011512447.1:c.*11G>T	XP_011510749.1:n.*11G>T
XM_011512447.3:c.*11G>T	XP_011510749.1:n.*11G>T
XM_017005748.2:c.*11G>T	XP_016861237.1:n.*11G>T
NM_181780.4:c.*11G>T MANE Select	NP_861445.4:n.*11G>T
NM_001085357.2:c.*11G>T	NP_001078826.1:n.*11G>T