Canonical Allele Identifier: CA11452113
Gene: BTLA HGNC NCBI

Linked Data

dbSNP Id: rs1982809
gnomAD v2: 3-112182740-A-G
gnomAD v3: 3-112463893-A-G
gnomAD v4: 3-112463893-A-G
MyVariant Identifiers: chr3:g.112182740A>G (hg19) chr3:g.112463893A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.112463893A>G , CM000665.2:g.112463893A>G GRCh38
NC_000003.11:g.112182740A>G , CM000665.1:g.112182740A>G GRCh37
NC_000003.10:g.113665430A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512447.3:c.*2215T>C XP_011510749.1:n.*2215T>C
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