Canonical Allele Identifier: CA353801202

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466175-T-G
• MyVariant Identifiers: chr3:g.112185022T>G (hg19) ; chr3:g.112466175T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466175T>G , CM000665.2:g.112466175T>G	GRCh38
NC_000003.11:g.112185022T>G , CM000665.1:g.112185022T>G	GRCh37
NC_000003.10:g.113667712T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.803A>C MANE Select	ENSP00000333919.5:p.Asn268Thr
ENST00000334529.9:c.803A>C	ENSP00000333919.5:p.Asn268Thr
ENST00000383680.4:c.659A>C	ENSP00000373178.4:p.Asn220Thr
ENST00000474965.1:n.307A>C
NM_001085357.1:c.659A>C	NP_001078826.1:p.Asn220Thr
NM_181780.3:c.803A>C	NP_861445.3:p.Asn268Thr
XM_011512446.1:c.821A>C	XP_011510748.1:p.Asn274Thr
XM_011512447.1:c.821A>C	XP_011510749.1:p.Asn274Thr
XM_011512447.3:c.821A>C	XP_011510749.1:p.Asn274Thr
XM_017005748.2:c.803A>C	XP_016861237.1:p.Asn268Thr
NM_181780.4:c.803A>C MANE Select	NP_861445.4:p.Asn268Thr
NM_001085357.2:c.659A>C	NP_001078826.1:p.Asn220Thr