Canonical Allele Identifier: CA314397231
Gene: LBP HGNC NCBI

Linked Data

dbSNP Id: rs982722426
MyVariant Identifiers: chr20:g.36992118C>T (hg19) chr20:g.38363464C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363464C>T , CM000682.2:g.38363464C>T GRCh38
NC_000020.10:g.36992118C>T , CM000682.1:g.36992118C>T GRCh37
NC_000020.9:g.36425532C>T NCBI36
NG_034239.1:g.22054C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-511C>T MANE Select ENSP00000217407.2:n.653-511C>T
ENST00000217407.2:c.653-511C>T ENSP00000217407.2:n.653-511C>T
NM_004139.4:c.653-511C>T NP_004130.2:n.653-511C>T
NM_004139.5:c.653-511C>T MANE Select NP_004130.2:n.653-511C>T
Search 100 bp 5'
Search 100 bp 3'