Canonical Allele Identifier: CA2340186825
Gene: LHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016162_49016173delinsCCACAGCGACAG , CM000681.2:g.49016162_49016173delinsCCACAGCGACAG GRCh38
NC_000019.9:g.49519419_49519430delinsCCACAGCGACAG , CM000681.1:g.49519419_49519430delinsCCACAGCGACAG GRCh37
NC_000019.8:g.54211231_54211242delinsCCACAGCGACAG NCBI36
NG_011464.1:g.5918_5929delinsCTGTCGCTGTGG
NG_033041.1:g.27264_27275delinsCCACAGCGACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.321_332delinsCTGTCGCTGTGG MANE Select ENSP00000497294.2:p.Ser107=
ENST00000649284.1:n.412_423delinsCTGTCGCTGTGG
ENST00000221421.6:c.321_332delinsCTGTCGCTGTGG ENSP00000221421.1:p.Ser107=
ENST00000391869.4:c.315_326delinsCTGTCGCTGTGG ENSP00000375742.4:p.Ser105=
NM_000894.2:c.321_332delinsCTGTCGCTGTGG NP_000885.1:p.Ser107=
XM_011526975.1:c.369_380delinsCTGTCGCTGTGG XP_011525277.1:p.Ser123=
NM_000894.3:c.321_332delinsCTGTCGCTGTGG MANE Select NP_000885.1:p.Ser107=