Canonical Allele Identifier: CA1017417722
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38360727A>C , CM000682.2:g.38360727A>C GRCh38
NG_034239.1:g.19317A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.612A>C MANE Select ENSP00000217407.2:p.Ser204=
ENST00000217407.2:c.612A>C ENSP00000217407.2:p.Ser204=
NM_004139.4:c.612A>C NP_004130.2:p.Ser204=
NM_004139.5:c.612A>C MANE Select NP_004130.2:p.Ser204=