Canonical Allele Identifier: CA309746626
Gene: LILRA2 HGNC NCBI
LILRA1 HGNC NCBI

Linked Data

dbSNP Id: rs532939298
MyVariant Identifiers: chr19:g.54587420G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54587420G>A , CM000681.2:g.54587420G>A GRCh38
NC_000019.8:g.59790699G>A NCBI36
NG_034038.1:g.19424G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000391738.8:c.*74G>A (LILRA2) MANE Select ENSP00000375618.3:n.*74G>A
ENST00000251376.7:c.*74G>A (LILRA2) ENSP00000251376.3:n.*74G>A
ENST00000251377.7:c.*74G>A (LILRA2) ENSP00000251377.3:n.*74G>A
ENST00000391738.7:c.*74G>A (LILRA2) ENSP00000375618.3:n.*74G>A
ENST00000472992.1:c.517G>A (LILRA2)
ENST00000618665.4:c.71-7245G>A (LILRA1) ENSP00000479482.1:n.71-7245G>A
NM_001130917.2:c.*74G>A (LILRA2) NP_001124389.2:n.*74G>A
NM_001290270.1:c.*74G>A (LILRA2) NP_001277199.1:n.*74G>A
NM_001290271.1:c.*261G>A (LILRA2) NP_001277200.1:n.*261G>A
NM_006866.3:c.*74G>A (LILRA2) NP_006857.2:n.*74G>A
XM_006722986.1:c.*261G>A (LILRA2) XP_006723049.1:n.*261G>A
XM_011526385.1:c.*74G>A (LILRA2) XP_011524687.1:n.*74G>A
XM_011526386.1:c.*261G>A (LILRA2) XP_011524688.1:n.*261G>A
XM_011526387.1:c.*74G>A (LILRA2) XP_011524689.1:n.*74G>A
XM_011526389.1:c.*261G>A (LILRA2) XP_011524691.1:n.*261G>A
XM_017026224.1:c.*261G>A (LILRA2) XP_016881713.1:n.*261G>A
NM_001130917.3:c.*74G>A (LILRA2) MANE Select NP_001124389.2:n.*74G>A
NM_001290271.2:c.*261G>A (LILRA2) NP_001277200.1:n.*261G>A
NM_006866.4:c.*74G>A (LILRA2) NP_006857.2:n.*74G>A