Canonical Allele Identifier: CA2340186784

Gene: LHB

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016142A= , CM000681.2:g.49016142A=	GRCh38
NC_000019.9:g.49519399A= , CM000681.1:g.49519399A=	GRCh37
NC_000019.8:g.54211211A=	NCBI36
NG_011464.1:g.5949T=
NG_033041.1:g.27244A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.352T= MANE Select	ENSP00000497294.2:p.Ser118=
ENST00000649284.1:n.443T=
ENST00000221421.6:c.352T=	ENSP00000221421.1:p.Ser118=
ENST00000391869.4:c.346T=	ENSP00000375742.4:p.Ser116=
NM_000894.2:c.352T=	NP_000885.1:p.Ser118=
XM_011526975.1:c.400T=	XP_011525277.1:p.Ser134=
NM_000894.3:c.352T= MANE Select	NP_000885.1:p.Ser118=