Canonical Allele Identifier: CA1293259771
Gene: LRP1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963709C= , CM000664.2:g.140963709C= GRCh38
NC_000002.11:g.141721278C= , CM000664.1:g.141721278C= GRCh37
NC_000002.10:g.141437748C= NCBI36
NG_051023.1:g.1173755G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.2888-11769G= MANE Select ENSP00000374135.3:n.2888-11769G=
ENST00000389484.7:c.2888-11769G= ENSP00000374135.3:n.2888-11769G=
ENST00000434794.1:c.323-11769G= ENSP00000413239.1:n.323-11769G=
ENST00000618808.4:c.2546-11769G= ENSP00000478868.1:n.2546-11769G=
NM_018557.2:c.2888-11769G= NP_061027.2:n.2888-11769G=
XM_011511352.1:c.2999-11769G= XP_011509654.1:n.2999-11769G=
XM_017004341.1:c.2498-11769G= XP_016859830.1:n.2498-11769G=
XR_001738778.1:n.4622-11769G=
NM_018557.3:c.2888-11769G= MANE Select NP_061027.2:n.2888-11769G=
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