Canonical Allele Identifier: CA635443644
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs1278752938
gnomAD v2: 20-36991821-CT-C
gnomAD v3: 20-38363167-CT-C
gnomAD v4: 20-38363167-CT-C
MyVariant Identifiers: chr20:g.36991822del (hg19) chr20:g.38363168del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363170del , CM000682.2:g.38363170del GRCh38
NC_000020.10:g.36991824del , CM000682.1:g.36991824del GRCh37
NC_000020.9:g.36425238del NCBI36
NG_034239.1:g.21760del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-805del MANE Select ENSP00000217407.2:n.653-805del
ENST00000217407.2:c.653-805del ENSP00000217407.2:n.653-805del
NM_004139.4:c.653-805del NP_004130.2:n.653-805del
NM_004139.5:c.653-805del MANE Select NP_004130.2:n.653-805del
Search 100 bp 5'
Search 100 bp 3'