Canonical Allele Identifier: CA406777186
Gene: LHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016150C>A , CM000681.2:g.49016150C>A GRCh38
NC_000019.9:g.49519407C>A , CM000681.1:g.49519407C>A GRCh37
NC_000019.8:g.54211219C>A NCBI36
NG_011464.1:g.5941G>T
NG_033041.1:g.27252C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.344G>T MANE Select ENSP00000497294.2:p.Arg115Leu
ENST00000649284.1:n.435G>T
ENST00000221421.6:c.344G>T ENSP00000221421.1:p.Arg115Leu
ENST00000391869.4:c.338G>T ENSP00000375742.4:p.Arg113Leu
NM_000894.2:c.344G>T NP_000885.1:p.Arg115Leu
XM_011526975.1:c.392G>T XP_011525277.1:p.Arg131Leu
NM_000894.3:c.344G>T MANE Select NP_000885.1:p.Arg115Leu