Canonical Allele Identifier: CA1293294619

Gene: LRP1B

Linked Data

• dbSNP Id: rs1698578355

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141037863C>A , CM000664.2:g.141037863C>A	GRCh38
NC_000002.11:g.141795432C>A , CM000664.1:g.141795432C>A	GRCh37
NC_000002.10:g.141511902C>A	NCBI36
NG_051023.1:g.1099601G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.1789+11123G>T MANE Select	ENSP00000374135.3:n.1789+11123G>T
ENST00000389484.7:c.1789+11123G>T	ENSP00000374135.3:n.1789+11123G>T
ENST00000434794.1:c.206-55587G>T	ENSP00000413239.1:n.206-55587G>T
ENST00000618808.4:c.1447+11123G>T	ENSP00000478868.1:n.1447+11123G>T
NM_018557.2:c.1789+11123G>T	NP_061027.2:n.1789+11123G>T
XM_011511352.1:c.1900+11123G>T	XP_011509654.1:n.1900+11123G>T
XM_017004341.1:c.1399+11123G>T	XP_016859830.1:n.1399+11123G>T
XR_001738778.1:n.3523+11123G>T
NM_018557.3:c.1789+11123G>T MANE Select	NP_061027.2:n.1789+11123G>T