Canonical Allele Identifier: CA2752443169
Gene: LRP1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.141037971G>C , CM000664.2:g.141037971G>C GRCh38
NC_000002.11:g.141795540G>C , CM000664.1:g.141795540G>C GRCh37
NC_000002.10:g.141512010G>C NCBI36
NG_051023.1:g.1099493C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389484.8:c.1789+11015C>G MANE Select ENSP00000374135.3:n.1789+11015C>G
ENST00000389484.7:c.1789+11015C>G ENSP00000374135.3:n.1789+11015C>G
ENST00000434794.1:c.206-55695C>G ENSP00000413239.1:n.206-55695C>G
ENST00000618808.4:c.1447+11015C>G ENSP00000478868.1:n.1447+11015C>G
NM_018557.2:c.1789+11015C>G NP_061027.2:n.1789+11015C>G
XM_011511352.1:c.1900+11015C>G XP_011509654.1:n.1900+11015C>G
XM_017004341.1:c.1399+11015C>G XP_016859830.1:n.1399+11015C>G
XR_001738778.1:n.3523+11015C>G
NM_018557.3:c.1789+11015C>G MANE Select NP_061027.2:n.1789+11015C>G
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