Canonical Allele Identifier: CA2340186983

Gene: LHB

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016036G= , CM000681.2:g.49016036G=	GRCh38
NC_000019.9:g.49519293G= , CM000681.1:g.49519293G=	GRCh37
NC_000019.8:g.54211105G=	NCBI36
NG_011464.1:g.6055C=
NG_033041.1:g.27138G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.*32C= MANE Select	ENSP00000497294.2:n.*32C=
ENST00000221421.6:c.458C=	ENSP00000221421.1:n.458C=
ENST00000391869.4:c.448C=	ENSP00000375742.4:p.Arg150=
NM_000894.2:c.*32C=	NP_000885.1:n.*32C=
XM_011526975.1:c.*32C=	XP_011525277.1:n.*32C=
NM_000894.3:c.*32C= MANE Select	NP_000885.1:n.*32C=