Canonical Allele Identifier: CA349158148

Gene: LRP2

Linked Data

• gnomAD v4: 2-169259067-T-C
• MyVariant Identifiers: chr2:g.170115577T>C (hg19) ; chr2:g.169259067T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259067T>C , CM000664.2:g.169259067T>C	GRCh38
NC_000002.11:g.170115577T>C , CM000664.1:g.170115577T>C	GRCh37
NC_000002.10:g.169823823T>C	NCBI36
NG_012634.1:g.108546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2471A>G MANE Select	ENSP00000496870.1:p.Tyr824Cys
ENST00000263816.7:c.2471A>G	ENSP00000263816.3:p.Tyr824Cys
ENST00000443831.1:c.2060A>G	ENSP00000409813.1:p.Tyr687Cys
NM_004525.2:c.2471A>G	NP_004516.2:p.Tyr824Cys
XM_011511183.1:c.2471A>G	XP_011509485.1:p.Tyr824Cys
XM_011511184.1:c.182A>G	XP_011509486.1:p.Tyr61Cys
XM_011511185.1:c.2471A>G	XP_011509487.1:p.Tyr824Cys
NM_004525.3:c.2471A>G MANE Select	NP_004516.2:p.Tyr824Cys
XM_011511183.3:c.2471A>G	XP_011509485.1:p.Tyr824Cys
XM_011511184.2:c.182A>G	XP_011509486.1:p.Tyr61Cys