Canonical Allele Identifier: CA508277098

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519352G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016095G>A , CM000681.2:g.49016095G>A	GRCh38
NC_000019.9:g.49519352G>A , CM000681.1:g.49519352G>A	GRCh37
NC_000019.8:g.54211164G>A	NCBI36
NG_011464.1:g.5996C>T
NG_033041.1:g.27197G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.399C>T MANE Select	ENSP00000497294.2:p.Pro133=
ENST00000649284.1:n.490C>T
ENST00000221421.6:c.399C>T	ENSP00000221421.1:p.Pro133=
ENST00000391869.4:c.393C>T	ENSP00000375742.4:p.Pro131=
NM_000894.2:c.399C>T	NP_000885.1:p.Pro133=
XM_011526975.1:c.447C>T	XP_011525277.1:p.Pro149=
NM_000894.3:c.399C>T MANE Select	NP_000885.1:p.Pro133=