Canonical Allele Identifier: CA1293294990
Gene: LRP1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.141038139T= , CM000664.2:g.141038139T= GRCh38
NC_000002.11:g.141795708T= , CM000664.1:g.141795708T= GRCh37
NC_000002.10:g.141512178T= NCBI36
NG_051023.1:g.1099325A=

Transcript Alleles

HGVS Amino-acid change
ENST00000389484.8:c.1789+10847A= MANE Select ENSP00000374135.3:n.1789+10847A=
ENST00000389484.7:c.1789+10847A= ENSP00000374135.3:n.1789+10847A=
ENST00000434794.1:c.206-55863A= ENSP00000413239.1:n.206-55863A=
ENST00000618808.4:c.1447+10847A= ENSP00000478868.1:n.1447+10847A=
NM_018557.2:c.1789+10847A= NP_061027.2:n.1789+10847A=
XM_011511352.1:c.1900+10847A= XP_011509654.1:n.1900+10847A=
XM_017004341.1:c.1399+10847A= XP_016859830.1:n.1399+10847A=
XR_001738778.1:n.3523+10847A=
NM_018557.3:c.1789+10847A= MANE Select NP_061027.2:n.1789+10847A=
Search 100 bp 5'
Search 100 bp 3'