Canonical Allele Identifier: CA309746438
Gene: LILRA2 HGNC NCBI

Linked Data

dbSNP Id: rs2241524
MyVariant Identifiers: chr19:g.54587200G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54587200G>C , CM000681.2:g.54587200G>C GRCh38
NC_000019.8:g.59790479G>C NCBI36
NG_034038.1:g.19204G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000391738.8:c.1307-1G>C MANE Select ENSP00000375618.3:p.=
ENST00000251376.7:c.1256-1G>C ENSP00000251376.3:p.=
ENST00000251377.7:c.1307-1G>C ENSP00000251377.3:p.=
ENST00000391737.3:c.1220-1G>C ENSP00000375617.1:p.=
ENST00000391738.7:c.1307-1G>C ENSP00000375618.3:p.=
ENST00000472992.1:n.298-1G>C
ENST00000618665.4:n.71-7465G>C ENSP00000479482.1:p.=
ENST00000629481.1:n.467-1G>C ENSP00000486483.1:p.=
NM_001130917.2:c.1307-1G>C NP_001124389.2:p.=
NM_001290270.1:c.1220-1G>C NP_001277199.1:p.=
NM_001290271.1:c.*42-1G>C NP_001277200.1:p.=
NM_006866.3:c.1256-1G>C NP_006857.2:p.=
XM_006722986.1:c.*42-1G>C XP_006723049.1:p.=
XM_011526385.1:c.1307-1G>C XP_011524687.1:p.=
XM_011526386.1:c.*42-1G>C XP_011524688.1:p.=
XM_011526387.1:c.1220-1G>C XP_011524689.1:p.=
XM_011526389.1:c.*42-1G>C XP_011524691.1:p.=
XM_017026224.1:c.*42-1G>C XP_016881713.1:p.=
NM_001130917.3:c.1307-1G>C MANE Select NP_001124389.2:p.=
NM_001290271.2:c.*42-1G>C NP_001277200.1:p.=
NM_006866.4:c.1256-1G>C NP_006857.2:p.=