Canonical Allele Identifier: CA1293259536
Gene: LRP1B HGNC NCBI

Linked Data

dbSNP Id: rs1696101208
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963483dup , CM000664.2:g.140963483dup GRCh38
NC_000002.11:g.141721052dup , CM000664.1:g.141721052dup GRCh37
NC_000002.10:g.141437522dup NCBI36
NG_051023.1:g.1173981dup

Transcript Alleles

HGVS Amino-acid change
ENST00000389484.8:c.2888-11543dup MANE Select ENSP00000374135.3:n.2888-11543dup
ENST00000389484.7:c.2888-11543dup ENSP00000374135.3:n.2888-11543dup
ENST00000434794.1:c.323-11543dup ENSP00000413239.1:n.323-11543dup
ENST00000618808.4:c.2546-11543dup ENSP00000478868.1:n.2546-11543dup
NM_018557.2:c.2888-11543dup NP_061027.2:n.2888-11543dup
XM_011511352.1:c.2999-11543dup XP_011509654.1:n.2999-11543dup
XM_017004341.1:c.2498-11543dup XP_016859830.1:n.2498-11543dup
XR_001738778.1:n.4622-11543dup
NM_018557.3:c.2888-11543dup MANE Select NP_061027.2:n.2888-11543dup
Search 100 bp 5'
Search 100 bp 3'