Canonical Allele Identifier: CA2556582283
Gene: LRP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.141038094G>T , CM000664.2:g.141038094G>T GRCh38
NC_000002.11:g.141795663G>T , CM000664.1:g.141795663G>T GRCh37
NC_000002.10:g.141512133G>T NCBI36
NG_051023.1:g.1099370C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000389484.8:c.1789+10892C>A MANE Select ENSP00000374135.3:n.1789+10892C>A
ENST00000389484.7:c.1789+10892C>A ENSP00000374135.3:n.1789+10892C>A
ENST00000434794.1:c.206-55818C>A ENSP00000413239.1:n.206-55818C>A
ENST00000618808.4:c.1447+10892C>A ENSP00000478868.1:n.1447+10892C>A
NM_018557.2:c.1789+10892C>A NP_061027.2:n.1789+10892C>A
XM_011511352.1:c.1900+10892C>A XP_011509654.1:n.1900+10892C>A
XM_017004341.1:c.1399+10892C>A XP_016859830.1:n.1399+10892C>A
XR_001738778.1:n.3523+10892C>A
NM_018557.3:c.1789+10892C>A MANE Select NP_061027.2:n.1789+10892C>A