Canonical Allele Identifier: CA2340186940

Gene: LHB

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016009G= , CM000681.2:g.49016009G=	GRCh38
NC_000019.9:g.49519266G= , CM000681.1:g.49519266G=	GRCh37
NC_000019.8:g.54211078G=	NCBI36
NG_011464.1:g.6082C=
NG_033041.1:g.27111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.*59C= MANE Select	ENSP00000497294.2:n.*59C=
ENST00000221421.6:c.485C=	ENSP00000221421.1:n.485C=
NM_000894.2:c.*59C=	NP_000885.1:n.*59C=
XM_011526975.1:c.*59C=	XP_011525277.1:n.*59C=
NM_000894.3:c.*59C= MANE Select	NP_000885.1:n.*59C=