Canonical Allele Identifier: CA406777197
Gene: LHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016153C>A , CM000681.2:g.49016153C>A GRCh38
NC_000019.9:g.49519410C>A , CM000681.1:g.49519410C>A GRCh37
NC_000019.8:g.54211222C>A NCBI36
NG_011464.1:g.5938G>T
NG_033041.1:g.27255C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.341G>T MANE Select ENSP00000497294.2:p.Arg114Leu
ENST00000649284.1:n.432G>T
ENST00000221421.6:c.341G>T ENSP00000221421.1:p.Arg114Leu
ENST00000391869.4:c.335G>T ENSP00000375742.4:p.Arg112Leu
NM_000894.2:c.341G>T NP_000885.1:p.Arg114Leu
XM_011526975.1:c.389G>T XP_011525277.1:p.Arg130Leu
NM_000894.3:c.341G>T MANE Select NP_000885.1:p.Arg114Leu