Canonical Allele Identifier: CA508277272

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519433G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016176G>T , CM000681.2:g.49016176G>T	GRCh38
NC_000019.9:g.49519433G>T , CM000681.1:g.49519433G>T	GRCh37
NC_000019.8:g.54211245G>T	NCBI36
NG_011464.1:g.5915C>A
NG_033041.1:g.27278G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.318C>A MANE Select	ENSP00000497294.2:p.Leu106=
ENST00000649284.1:n.409C>A
ENST00000221421.6:c.318C>A	ENSP00000221421.1:p.Leu106=
ENST00000391869.4:c.312C>A	ENSP00000375742.4:p.Leu104=
NM_000894.2:c.318C>A	NP_000885.1:p.Leu106=
XM_011526975.1:c.366C>A	XP_011525277.1:p.Leu122=
NM_000894.3:c.318C>A MANE Select	NP_000885.1:p.Leu106=