Canonical Allele Identifier: CA1393855013

Gene: BTLA

Linked Data

• dbSNP Id: rs1576674731
• gnomAD v4: 3-112466086-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466086C>T , CM000665.2:g.112466086C>T	GRCh38
NC_000003.11:g.112184933C>T , CM000665.1:g.112184933C>T	GRCh37
NC_000003.10:g.113667623C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.*22G>A MANE Select	ENSP00000333919.5:n.*22G>A
ENST00000334529.9:c.*22G>A	ENSP00000333919.5:n.*22G>A
ENST00000474965.1:n.396G>A
NM_001085357.1:c.*22G>A	NP_001078826.1:n.*22G>A
NM_181780.3:c.*22G>A	NP_861445.3:n.*22G>A
XM_011512446.1:c.*22G>A	XP_011510748.1:n.*22G>A
XM_011512447.1:c.*22G>A	XP_011510749.1:n.*22G>A
XM_011512447.3:c.*22G>A	XP_011510749.1:n.*22G>A
XM_017005748.2:c.*22G>A	XP_016861237.1:n.*22G>A
NM_181780.4:c.*22G>A MANE Select	NP_861445.4:n.*22G>A
NM_001085357.2:c.*22G>A	NP_001078826.1:n.*22G>A