Canonical Allele Identifier: CA57289625

Gene: LRP1B

Linked Data

• dbSNP Id: rs919509737
• MyVariant Identifiers: chr2:g.141795642G>A (hg19) ; chr2:g.141038073G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038073G>A , CM000664.2:g.141038073G>A	GRCh38
NC_000002.11:g.141795642G>A , CM000664.1:g.141795642G>A	GRCh37
NC_000002.10:g.141512112G>A	NCBI36
NG_051023.1:g.1099391C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10913C>T MANE Select	ENSP00000374135.3:n.1789+10913C>T
ENST00000389484.7:c.1789+10913C>T	ENSP00000374135.3:n.1789+10913C>T
ENST00000434794.1:c.206-55797C>T	ENSP00000413239.1:n.206-55797C>T
ENST00000618808.4:c.1447+10913C>T	ENSP00000478868.1:n.1447+10913C>T
NM_018557.2:c.1789+10913C>T	NP_061027.2:n.1789+10913C>T
XM_011511352.1:c.1900+10913C>T	XP_011509654.1:n.1900+10913C>T
XM_017004341.1:c.1399+10913C>T	XP_016859830.1:n.1399+10913C>T
XR_001738778.1:n.3523+10913C>T
NM_018557.3:c.1789+10913C>T MANE Select	NP_061027.2:n.1789+10913C>T