Canonical Allele Identifier: CA508277265

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519418T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016161T>C , CM000681.2:g.49016161T>C	GRCh38
NC_000019.9:g.49519418T>C , CM000681.1:g.49519418T>C	GRCh37
NC_000019.8:g.54211230T>C	NCBI36
NG_011464.1:g.5930A>G
NG_033041.1:g.27263T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.333A>G MANE Select	ENSP00000497294.2:p.Gly111=
ENST00000649284.1:n.424A>G
ENST00000221421.6:c.333A>G	ENSP00000221421.1:p.Gly111=
ENST00000391869.4:c.327A>G	ENSP00000375742.4:p.Gly109=
NM_000894.2:c.333A>G	NP_000885.1:p.Gly111=
XM_011526975.1:c.381A>G	XP_011525277.1:p.Gly127=
NM_000894.3:c.333A>G MANE Select	NP_000885.1:p.Gly111=