Canonical Allele Identifier: CA2340186797

Gene: LHB

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.341G= MANE Select	ENSP00000497294.2:p.Arg114=
ENST00000649284.1:n.432G=
ENST00000221421.6:c.341G=	ENSP00000221421.1:p.Arg114=
ENST00000391869.4:c.335G=	ENSP00000375742.4:p.Arg112=
NM_000894.2:c.341G=	NP_000885.1:p.Arg114=
XM_011526975.1:c.389G=	XP_011525277.1:p.Arg130=
NM_000894.3:c.341G= MANE Select	NP_000885.1:p.Arg114=