Canonical Allele Identifier: CA406777227
Gene: LHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016163C>G , CM000681.2:g.49016163C>G GRCh38
NC_000019.9:g.49519420C>G , CM000681.1:g.49519420C>G GRCh37
NC_000019.8:g.54211232C>G NCBI36
NG_011464.1:g.5928G>C
NG_033041.1:g.27265C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.331G>C MANE Select ENSP00000497294.2:p.Gly111Arg
ENST00000649284.1:n.422G>C
ENST00000221421.6:c.331G>C ENSP00000221421.1:p.Gly111Arg
ENST00000391869.4:c.325G>C ENSP00000375742.4:p.Gly109Arg
NM_000894.2:c.331G>C NP_000885.1:p.Gly111Arg
XM_011526975.1:c.379G>C XP_011525277.1:p.Gly127Arg
NM_000894.3:c.331G>C MANE Select NP_000885.1:p.Gly111Arg