Canonical Allele Identifier: CA757909508

Gene: LRP1B

Linked Data

• dbSNP Id: rs1238844476
• MyVariant Identifiers: chr2:g.141795676T>C (hg19) ; chr2:g.141038107T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038107T>C , CM000664.2:g.141038107T>C	GRCh38
NC_000002.11:g.141795676T>C , CM000664.1:g.141795676T>C	GRCh37
NC_000002.10:g.141512146T>C	NCBI36
NG_051023.1:g.1099357A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10879A>G MANE Select	ENSP00000374135.3:n.1789+10879A>G
ENST00000389484.7:c.1789+10879A>G	ENSP00000374135.3:n.1789+10879A>G
ENST00000434794.1:c.206-55831A>G	ENSP00000413239.1:n.206-55831A>G
ENST00000618808.4:c.1447+10879A>G	ENSP00000478868.1:n.1447+10879A>G
NM_018557.2:c.1789+10879A>G	NP_061027.2:n.1789+10879A>G
XM_011511352.1:c.1900+10879A>G	XP_011509654.1:n.1900+10879A>G
XM_017004341.1:c.1399+10879A>G	XP_016859830.1:n.1399+10879A>G
XR_001738778.1:n.3523+10879A>G
NM_018557.3:c.1789+10879A>G MANE Select	NP_061027.2:n.1789+10879A>G