Canonical Allele Identifier: CA1293259278
Gene: LRP1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963325G= , CM000664.2:g.140963325G= GRCh38
NC_000002.11:g.141720894G= , CM000664.1:g.141720894G= GRCh37
NC_000002.10:g.141437364G= NCBI36
NG_051023.1:g.1174139C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.2888-11385C= MANE Select ENSP00000374135.3:n.2888-11385C=
ENST00000389484.7:c.2888-11385C= ENSP00000374135.3:n.2888-11385C=
ENST00000434794.1:c.323-11385C= ENSP00000413239.1:n.323-11385C=
ENST00000618808.4:c.2546-11385C= ENSP00000478868.1:n.2546-11385C=
NM_018557.2:c.2888-11385C= NP_061027.2:n.2888-11385C=
XM_011511352.1:c.2999-11385C= XP_011509654.1:n.2999-11385C=
XM_017004341.1:c.2498-11385C= XP_016859830.1:n.2498-11385C=
XR_001738778.1:n.4622-11385C=
NM_018557.3:c.2888-11385C= MANE Select NP_061027.2:n.2888-11385C=
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