Canonical Allele Identifier: CA1293259370
Gene: LRP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963415G= , CM000664.2:g.140963415G= GRCh38
NC_000002.11:g.141720984G= , CM000664.1:g.141720984G= GRCh37
NC_000002.10:g.141437454G= NCBI36
NG_051023.1:g.1174049C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.2888-11475C= MANE Select ENSP00000374135.3:n.2888-11475C=
ENST00000389484.7:c.2888-11475C= ENSP00000374135.3:n.2888-11475C=
ENST00000434794.1:c.323-11475C= ENSP00000413239.1:n.323-11475C=
ENST00000618808.4:c.2546-11475C= ENSP00000478868.1:n.2546-11475C=
NM_018557.2:c.2888-11475C= NP_061027.2:n.2888-11475C=
XM_011511352.1:c.2999-11475C= XP_011509654.1:n.2999-11475C=
XM_017004341.1:c.2498-11475C= XP_016859830.1:n.2498-11475C=
XR_001738778.1:n.4622-11475C=
NM_018557.3:c.2888-11475C= MANE Select NP_061027.2:n.2888-11475C=