Canonical Allele Identifier: CA2539366
Gene: BTLA HGNC NCBI

Linked Data

dbSNP Id: rs16859633

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.112479488T>C , CM000665.2:g.112479488T>C GRCh38
NC_000003.11:g.112198335T>C , CM000665.1:g.112198335T>C GRCh37
NC_000003.10:g.113681025T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000334529.10:c.370A>G MANE Select ENSP00000333919.5:p.Ile124Val
ENST00000334529.9:c.370A>G ENSP00000333919.5:p.Ile124Val
ENST00000383680.4:c.370A>G ENSP00000373178.4:p.Ile124Val
NM_001085357.1:c.370A>G NP_001078826.1:p.Ile124Val
NM_181780.3:c.370A>G NP_861445.3:p.Ile124Val
XM_011512446.1:c.370A>G XP_011510748.1:p.Ile124Val
XM_011512447.1:c.370A>G XP_011510749.1:p.Ile124Val
XM_011512447.3:c.370A>G XP_011510749.1:p.Ile124Val
XM_017005748.2:c.370A>G XP_016861237.1:p.Ile124Val
NM_181780.4:c.370A>G MANE Select NP_861445.4:p.Ile124Val
NM_001085357.2:c.370A>G NP_001078826.1:p.Ile124Val