Canonical Allele Identifier: CA57289622

Gene: LRP1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038051A>G , CM000664.2:g.141038051A>G	GRCh38
NC_000002.11:g.141795620A>G , CM000664.1:g.141795620A>G	GRCh37
NC_000002.10:g.141512090A>G	NCBI36
NG_051023.1:g.1099413T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.1789+10935T>C MANE Select	ENSP00000374135.3:n.1789+10935T>C
ENST00000389484.7:c.1789+10935T>C	ENSP00000374135.3:n.1789+10935T>C
ENST00000434794.1:c.206-55775T>C	ENSP00000413239.1:n.206-55775T>C
ENST00000618808.4:c.1447+10935T>C	ENSP00000478868.1:n.1447+10935T>C
NM_018557.2:c.1789+10935T>C	NP_061027.2:n.1789+10935T>C
XM_011511352.1:c.1900+10935T>C	XP_011509654.1:n.1900+10935T>C
XM_017004341.1:c.1399+10935T>C	XP_016859830.1:n.1399+10935T>C
XR_001738778.1:n.3523+10935T>C
NM_018557.3:c.1789+10935T>C MANE Select	NP_061027.2:n.1789+10935T>C