Canonical Allele Identifier: CA536106313
Gene: LRP1B HGNC NCBI

Linked Data

dbSNP Id: rs1188771649
gnomAD v2: 2-141721234-A-G
MyVariant Identifiers: chr2:g.141721234A>G (hg19) chr2:g.140963665A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963665A>G , CM000664.2:g.140963665A>G GRCh38
NC_000002.11:g.141721234A>G , CM000664.1:g.141721234A>G GRCh37
NC_000002.10:g.141437704A>G NCBI36
NG_051023.1:g.1173799T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389484.8:c.2888-11725T>C MANE Select ENSP00000374135.3:n.2888-11725T>C
ENST00000389484.7:c.2888-11725T>C ENSP00000374135.3:n.2888-11725T>C
ENST00000434794.1:c.323-11725T>C ENSP00000413239.1:n.323-11725T>C
ENST00000618808.4:c.2546-11725T>C ENSP00000478868.1:n.2546-11725T>C
NM_018557.2:c.2888-11725T>C NP_061027.2:n.2888-11725T>C
XM_011511352.1:c.2999-11725T>C XP_011509654.1:n.2999-11725T>C
XM_017004341.1:c.2498-11725T>C XP_016859830.1:n.2498-11725T>C
XR_001738778.1:n.4622-11725T>C
NM_018557.3:c.2888-11725T>C MANE Select NP_061027.2:n.2888-11725T>C
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