Canonical Allele Identifier: CA1293294672
Gene: LRP1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.141037896T= , CM000664.2:g.141037896T= GRCh38
NC_000002.11:g.141795465T= , CM000664.1:g.141795465T= GRCh37
NC_000002.10:g.141511935T= NCBI36
NG_051023.1:g.1099568A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.1789+11090A= MANE Select ENSP00000374135.3:n.1789+11090A=
ENST00000389484.7:c.1789+11090A= ENSP00000374135.3:n.1789+11090A=
ENST00000434794.1:c.206-55620A= ENSP00000413239.1:n.206-55620A=
ENST00000618808.4:c.1447+11090A= ENSP00000478868.1:n.1447+11090A=
NM_018557.2:c.1789+11090A= NP_061027.2:n.1789+11090A=
XM_011511352.1:c.1900+11090A= XP_011509654.1:n.1900+11090A=
XM_017004341.1:c.1399+11090A= XP_016859830.1:n.1399+11090A=
XR_001738778.1:n.3523+11090A=
NM_018557.3:c.1789+11090A= MANE Select NP_061027.2:n.1789+11090A=
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