Canonical Allele Identifier: CA406777297

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519438C>T (hg19) ; chr19:g.49016181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016181C>T , CM000681.2:g.49016181C>T	GRCh38
NC_000019.9:g.49519438C>T , CM000681.1:g.49519438C>T	GRCh37
NC_000019.8:g.54211250C>T	NCBI36
NG_011464.1:g.5910G>A
NG_033041.1:g.27283C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.313G>A MANE Select	ENSP00000497294.2:p.Ala105Thr
ENST00000649284.1:n.404G>A
ENST00000221421.6:c.313G>A	ENSP00000221421.1:p.Ala105Thr
ENST00000391869.4:c.307G>A	ENSP00000375742.4:p.Ala103Thr
NM_000894.2:c.313G>A	NP_000885.1:p.Ala105Thr
XM_011526975.1:c.361G>A	XP_011525277.1:p.Ala121Thr
NM_000894.3:c.313G>A MANE Select	NP_000885.1:p.Ala105Thr