Canonical Allele Identifier: CA2340186918

Gene: LHB

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016221G= , CM000681.2:g.49016221G=	GRCh38
NC_000019.9:g.49519478G= , CM000681.1:g.49519478G=	GRCh37
NC_000019.8:g.54211290G=	NCBI36
NG_011464.1:g.5870C=
NG_033041.1:g.27323G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.273C= MANE Select	ENSP00000497294.2:p.Gly91=
ENST00000649284.1:n.364C=
ENST00000221421.6:c.273C=	ENSP00000221421.1:p.Gly91=
ENST00000391869.4:c.267C=	ENSP00000375742.4:p.Gly89=
NM_000894.2:c.273C=	NP_000885.1:p.Gly91=
XM_011526975.1:c.321C=	XP_011525277.1:p.Gly107=
NM_000894.3:c.273C= MANE Select	NP_000885.1:p.Gly91=