Canonical Allele Identifier: CA2666960697

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466102-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466102A>G , CM000665.2:g.112466102A>G	GRCh38
NC_000003.11:g.112184949A>G , CM000665.1:g.112184949A>G	GRCh37
NC_000003.10:g.113667639A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.*6T>C MANE Select	ENSP00000333919.5:n.*6T>C
ENST00000334529.9:c.*6T>C	ENSP00000333919.5:n.*6T>C
ENST00000474965.1:n.380T>C
NM_001085357.1:c.*6T>C	NP_001078826.1:n.*6T>C
NM_181780.3:c.*6T>C	NP_861445.3:n.*6T>C
XM_011512446.1:c.*6T>C	XP_011510748.1:n.*6T>C
XM_011512447.1:c.*6T>C	XP_011510749.1:n.*6T>C
XM_011512447.3:c.*6T>C	XP_011510749.1:n.*6T>C
XM_017005748.2:c.*6T>C	XP_016861237.1:n.*6T>C
NM_181780.4:c.*6T>C MANE Select	NP_861445.4:n.*6T>C
NM_001085357.2:c.*6T>C	NP_001078826.1:n.*6T>C