Canonical Allele Identifier: CA1293259586
Gene: LRP1B HGNC NCBI

Linked Data

dbSNP Id: rs1696102474

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963522T>C , CM000664.2:g.140963522T>C GRCh38
NC_000002.11:g.141721091T>C , CM000664.1:g.141721091T>C GRCh37
NC_000002.10:g.141437561T>C NCBI36
NG_051023.1:g.1173942A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389484.8:c.2888-11582A>G MANE Select ENSP00000374135.3:n.2888-11582A>G
ENST00000389484.7:c.2888-11582A>G ENSP00000374135.3:n.2888-11582A>G
ENST00000434794.1:c.323-11582A>G ENSP00000413239.1:n.323-11582A>G
ENST00000618808.4:c.2546-11582A>G ENSP00000478868.1:n.2546-11582A>G
NM_018557.2:c.2888-11582A>G NP_061027.2:n.2888-11582A>G
XM_011511352.1:c.2999-11582A>G XP_011509654.1:n.2999-11582A>G
XM_017004341.1:c.2498-11582A>G XP_016859830.1:n.2498-11582A>G
XR_001738778.1:n.4622-11582A>G
NM_018557.3:c.2888-11582A>G MANE Select NP_061027.2:n.2888-11582A>G