Canonical Allele Identifier: CA56698582

Gene: LRP1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140604489A>G , CM000664.2:g.140604489A>G	GRCh38
NC_000002.11:g.141362058A>G , CM000664.1:g.141362058A>G	GRCh37
NC_000002.10:g.141078528A>G	NCBI36
NG_051023.1:g.1532975T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.6800-2850T>C MANE Select	ENSP00000374135.3:n.6800-2850T>C
ENST00000389484.7:c.6800-2850T>C	ENSP00000374135.3:n.6800-2850T>C
ENST00000618808.4:c.6458-2850T>C	ENSP00000478868.1:n.6458-2850T>C
NM_018557.2:c.6800-2850T>C	NP_061027.2:n.6800-2850T>C
XM_011511352.1:c.6911-2850T>C	XP_011509654.1:n.6911-2850T>C
XM_017004341.1:c.6410-2850T>C	XP_016859830.1:n.6410-2850T>C
XM_017004342.1:c.1652-2850T>C	XP_016859831.1:n.1652-2850T>C
XR_001738778.1:n.8534-2850T>C
NM_018557.3:c.6800-2850T>C MANE Select	NP_061027.2:n.6800-2850T>C