Canonical Allele Identifier: CA2340186766

Gene: LHB

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016127G= , CM000681.2:g.49016127G=	GRCh38
NC_000019.9:g.49519384G= , CM000681.1:g.49519384G=	GRCh37
NC_000019.8:g.54211196G=	NCBI36
NG_011464.1:g.5964C=
NG_033041.1:g.27229G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.367C= MANE Select	ENSP00000497294.2:p.Pro123=
ENST00000649284.1:n.458C=
ENST00000221421.6:c.367C=	ENSP00000221421.1:p.Pro123=
ENST00000391869.4:c.361C=	ENSP00000375742.4:p.Pro121=
NM_000894.2:c.367C=	NP_000885.1:p.Pro123=
XM_011526975.1:c.415C=	XP_011525277.1:p.Pro139=
NM_000894.3:c.367C= MANE Select	NP_000885.1:p.Pro123=