Canonical Allele Identifier: CA744180613
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs1426244182
gnomAD v3: 20-38373021-CACCATGTG-C
gnomAD v4: 20-38373021-CACCATGTG-C
MyVariant Identifiers: chr20:g.37001666_37001673del (hg19) chr20:g.38373022_38373029del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38373022_38373029del , CM000682.2:g.38373022_38373029del GRCh38
NC_000020.10:g.37001666_37001673del , CM000682.1:g.37001666_37001673del GRCh37
NC_000020.9:g.36435080_36435087del NCBI36
NG_034239.1:g.31612_31619del

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.1261-50_1261-43del MANE Select ENSP00000217407.2:n.1261-50_1261-43del
ENST00000217407.2:c.1261-50_1261-43del ENSP00000217407.2:n.1261-50_1261-43del
NM_004139.4:c.1261-50_1261-43del NP_004130.2:n.1261-50_1261-43del
NM_004139.5:c.1261-50_1261-43del MANE Select NP_004130.2:n.1261-50_1261-43del
Search 100 bp 5'
Search 100 bp 3'