Canonical Allele Identifier: CA757914916

Gene: LRP1B

Linked Data

• dbSNP Id: rs1459785428
• gnomAD v3: 2-140963201-T-TA
• gnomAD v4: 2-140963201-T-TA
• MyVariant Identifiers: chr2:g.141720770_141720771insA (hg19) ; chr2:g.140963201_140963202insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963203dup , CM000664.2:g.140963203dup	GRCh38
NC_000002.11:g.141720772dup , CM000664.1:g.141720772dup	GRCh37
NC_000002.10:g.141437242dup	NCBI36
NG_051023.1:g.1174262dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11262dup MANE Select	ENSP00000374135.3:n.2888-11262dup
ENST00000389484.7:c.2888-11262dup	ENSP00000374135.3:n.2888-11262dup
ENST00000434794.1:c.323-11262dup	ENSP00000413239.1:n.323-11262dup
ENST00000618808.4:c.2546-11262dup	ENSP00000478868.1:n.2546-11262dup
NM_018557.2:c.2888-11262dup	NP_061027.2:n.2888-11262dup
XM_011511352.1:c.2999-11262dup	XP_011509654.1:n.2999-11262dup
XM_017004341.1:c.2498-11262dup	XP_016859830.1:n.2498-11262dup
XR_001738778.1:n.4622-11262dup
NM_018557.3:c.2888-11262dup MANE Select	NP_061027.2:n.2888-11262dup