Canonical Allele Identifier: CA897214250

Gene: BTLA

Linked Data

• dbSNP Id: rs35030966
• gnomAD v4: 3-112466084-TC-T
• MyVariant Identifiers: chr3:g.112184932del (hg19) ; chr3:g.112466085del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466087del , CM000665.2:g.112466087del	GRCh38
NC_000003.11:g.112184934del , CM000665.1:g.112184934del	GRCh37
NC_000003.10:g.113667624del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.*23del MANE Select	ENSP00000333919.5:n.*23del
ENST00000334529.9:c.*23del	ENSP00000333919.5:n.*23del
ENST00000474965.1:n.397del
NM_001085357.1:c.*23del	NP_001078826.1:n.*23del
NM_181780.3:c.*23del	NP_861445.3:n.*23del
XM_011512446.1:c.*23del	XP_011510748.1:n.*23del
XM_011512447.1:c.*23del	XP_011510749.1:n.*23del
XM_011512447.3:c.*23del	XP_011510749.1:n.*23del
XM_017005748.2:c.*23del	XP_016861237.1:n.*23del
NM_181780.4:c.*23del MANE Select	NP_861445.4:n.*23del
NM_001085357.2:c.*23del	NP_001078826.1:n.*23del