Canonical Allele Identifier: CA46492449
Gene: LRPPRC HGNC NCBI

Linked Data

dbSNP Id: rs1051682935
MyVariant Identifiers: chr2:g.44113780G>A (hg19) chr2:g.43886641G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43886641G>A , CM000664.2:g.43886641G>A GRCh38
NC_000002.11:g.44113780G>A , CM000664.1:g.44113780G>A GRCh37
NC_000002.10:g.43967284G>A NCBI36
NG_008247.1:g.114365C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682612.1:c.2911C>T
ENST00000684454.1:n.10008C>T
ENST00000260665.12:c.*1959C>T MANE Select ENSP00000260665.7:n.*1959C>T
ENST00000260665.11:c.*1959C>T ENSP00000260665.7:n.*1959C>T
NM_133259.3:c.*1959C>T NP_573566.2:n.*1959C>T
XR_002958896.1:n.6326C>T
NM_133259.4:c.*1959C>T MANE Select NP_573566.2:n.*1959C>T
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