Canonical Allele Identifier: CA406777327

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519450A>T (hg19) ; chr19:g.49016193A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016193A>T , CM000681.2:g.49016193A>T	GRCh38
NC_000019.9:g.49519450A>T , CM000681.1:g.49519450A>T	GRCh37
NC_000019.8:g.54211262A>T	NCBI36
NG_011464.1:g.5898T>A
NG_033041.1:g.27295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.301T>A MANE Select	ENSP00000497294.2:p.Ser101Thr
ENST00000649284.1:n.392T>A
ENST00000221421.6:c.301T>A	ENSP00000221421.1:p.Ser101Thr
ENST00000391869.4:c.295T>A	ENSP00000375742.4:p.Ser99Thr
NM_000894.2:c.301T>A	NP_000885.1:p.Ser101Thr
XM_011526975.1:c.349T>A	XP_011525277.1:p.Ser117Thr
NM_000894.3:c.301T>A MANE Select	NP_000885.1:p.Ser101Thr