Canonical Allele Identifier: CA2814675262
Gene: LHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016124del , CM000681.2:g.49016124del GRCh38
NC_000019.9:g.49519381del , CM000681.1:g.49519381del GRCh37
NC_000019.8:g.54211193del NCBI36
NG_011464.1:g.5969del
NG_033041.1:g.27226del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.372del MANE Select ENSP00000497294.2:p.Asp125ThrfsTer4
ENST00000649284.1:n.463del
ENST00000221421.6:c.372del ENSP00000221421.1:p.Asp125ThrfsTer4
ENST00000391869.4:c.366del ENSP00000375742.4:p.Asp123ThrfsTer4
NM_000894.2:c.372del NP_000885.1:p.Asp125ThrfsTer4
XM_011526975.1:c.420del XP_011525277.1:p.Asp141ThrfsTer4
NM_000894.3:c.372del MANE Select NP_000885.1:p.Asp125ThrfsTer4