Canonical Allele Identifier: CA1017432325
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs2076811964
gnomAD v3: 20-38349256-C-T
gnomAD v4: 20-38349256-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38349256C>T , CM000682.2:g.38349256C>T GRCh38
NC_000020.10:g.36977659C>T , CM000682.1:g.36977659C>T GRCh37
NC_000020.9:g.36411073C>T NCBI36
NG_034239.1:g.7846C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217407.3:c.125-292C>T MANE Select ENSP00000217407.2:n.125-292C>T
ENST00000217407.2:c.125-292C>T ENSP00000217407.2:n.125-292C>T
NM_004139.4:c.125-292C>T NP_004130.2:n.125-292C>T
NM_004139.5:c.125-292C>T MANE Select NP_004130.2:n.125-292C>T
Search 100 bp 5'
Search 100 bp 3'