Canonical Allele Identifier: CA744180616
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs1487767438
gnomAD v3: 20-38373024-C-A
gnomAD v4: 20-38373024-C-A
MyVariant Identifiers: chr20:g.37001668C>A (hg19) chr20:g.38373024C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38373024C>A , CM000682.2:g.38373024C>A GRCh38
NC_000020.10:g.37001668C>A , CM000682.1:g.37001668C>A GRCh37
NC_000020.9:g.36435082C>A NCBI36
NG_034239.1:g.31614C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.1261-48C>A MANE Select ENSP00000217407.2:n.1261-48C>A
ENST00000217407.2:c.1261-48C>A ENSP00000217407.2:n.1261-48C>A
NM_004139.4:c.1261-48C>A NP_004130.2:n.1261-48C>A
NM_004139.5:c.1261-48C>A MANE Select NP_004130.2:n.1261-48C>A
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