Canonical Allele Identifier: CA406777146

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519396C>A (hg19) ; chr19:g.49016139C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016139C>A , CM000681.2:g.49016139C>A	GRCh38
NC_000019.9:g.49519396C>A , CM000681.1:g.49519396C>A	GRCh37
NC_000019.8:g.54211208C>A	NCBI36
NG_011464.1:g.5952G>T
NG_033041.1:g.27241C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.355G>T MANE Select	ENSP00000497294.2:p.Asp119Tyr
ENST00000649284.1:n.446G>T
ENST00000221421.6:c.355G>T	ENSP00000221421.1:p.Asp119Tyr
ENST00000391869.4:c.349G>T	ENSP00000375742.4:p.Asp117Tyr
NM_000894.2:c.355G>T	NP_000885.1:p.Asp119Tyr
XM_011526975.1:c.403G>T	XP_011525277.1:p.Asp135Tyr
NM_000894.3:c.355G>T MANE Select	NP_000885.1:p.Asp119Tyr