Canonical Allele Identifier: CA1037173629

Gene: LRP1B

Linked Data

• dbSNP Id: rs10928082
• gnomAD v3: 2-140963590-C-G
• gnomAD v4: 2-140963590-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963590C>G , CM000664.2:g.140963590C>G	GRCh38
NC_000002.11:g.141721159C>G , CM000664.1:g.141721159C>G	GRCh37
NC_000002.10:g.141437629C>G	NCBI36
NG_051023.1:g.1173874G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.2888-11650G>C MANE Select	ENSP00000374135.3:n.2888-11650G>C
ENST00000389484.7:c.2888-11650G>C	ENSP00000374135.3:n.2888-11650G>C
ENST00000434794.1:c.323-11650G>C	ENSP00000413239.1:n.323-11650G>C
ENST00000618808.4:c.2546-11650G>C	ENSP00000478868.1:n.2546-11650G>C
NM_018557.2:c.2888-11650G>C	NP_061027.2:n.2888-11650G>C
XM_011511352.1:c.2999-11650G>C	XP_011509654.1:n.2999-11650G>C
XM_017004341.1:c.2498-11650G>C	XP_016859830.1:n.2498-11650G>C
XR_001738778.1:n.4622-11650G>C
NM_018557.3:c.2888-11650G>C MANE Select	NP_061027.2:n.2888-11650G>C