Canonical Allele Identifier: CA508277101

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519361A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016104A>G , CM000681.2:g.49016104A>G	GRCh38
NC_000019.9:g.49519361A>G , CM000681.1:g.49519361A>G	GRCh37
NC_000019.8:g.54211173A>G	NCBI36
NG_011464.1:g.5987T>C
NG_033041.1:g.27206A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.390T>C MANE Select	ENSP00000497294.2:p.Cys130=
ENST00000649284.1:n.481T>C
ENST00000221421.6:c.390T>C	ENSP00000221421.1:p.Cys130=
ENST00000391869.4:c.384T>C	ENSP00000375742.4:p.Cys128=
NM_000894.2:c.390T>C	NP_000885.1:p.Cys130=
XM_011526975.1:c.438T>C	XP_011525277.1:p.Cys146=
NM_000894.3:c.390T>C MANE Select	NP_000885.1:p.Cys130=