Canonical Allele Identifier: CA314388189
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs116923710
gnomAD v2: 20-36977673-G-A
gnomAD v3: 20-38349270-G-A
gnomAD v4: 20-38349270-G-A
MyVariant Identifiers: chr20:g.36977673G>A (hg19) chr20:g.38349270G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349270G>A , CM000682.2:g.38349270G>A GRCh38
NC_000020.10:g.36977673G>A , CM000682.1:g.36977673G>A GRCh37
NC_000020.9:g.36411087G>A NCBI36
NG_034239.1:g.7860G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-278G>A MANE Select ENSP00000217407.2:n.125-278G>A
ENST00000217407.2:c.125-278G>A ENSP00000217407.2:n.125-278G>A
NM_004139.4:c.125-278G>A NP_004130.2:n.125-278G>A
NM_004139.5:c.125-278G>A MANE Select NP_004130.2:n.125-278G>A
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