Canonical Allele Identifier: CA2666960681
Gene: BTLA HGNC NCBI

Linked Data

gnomAD v4: 3-112466079-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.112466079A>T , CM000665.2:g.112466079A>T GRCh38
NC_000003.11:g.112184926A>T , CM000665.1:g.112184926A>T GRCh37
NC_000003.10:g.113667616A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334529.10:c.*29T>A MANE Select ENSP00000333919.5:n.*29T>A
ENST00000334529.9:c.*29T>A ENSP00000333919.5:n.*29T>A
ENST00000474965.1:n.403T>A
NM_001085357.1:c.*29T>A NP_001078826.1:n.*29T>A
NM_181780.3:c.*29T>A NP_861445.3:n.*29T>A
XM_011512446.1:c.*29T>A XP_011510748.1:n.*29T>A
XM_011512447.1:c.*29T>A XP_011510749.1:n.*29T>A
XM_011512447.3:c.*29T>A XP_011510749.1:n.*29T>A
XM_017005748.2:c.*29T>A XP_016861237.1:n.*29T>A
NM_181780.4:c.*29T>A MANE Select NP_861445.4:n.*29T>A
NM_001085357.2:c.*29T>A NP_001078826.1:n.*29T>A
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