Canonical Allele Identifier: CA406777216

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519416G>T (hg19) ; chr19:g.49016159G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016159G>T , CM000681.2:g.49016159G>T	GRCh38
NC_000019.9:g.49519416G>T , CM000681.1:g.49519416G>T	GRCh37
NC_000019.8:g.54211228G>T	NCBI36
NG_011464.1:g.5932C>A
NG_033041.1:g.27261G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.335C>A MANE Select	ENSP00000497294.2:p.Pro112His
ENST00000649284.1:n.426C>A
ENST00000221421.6:c.335C>A	ENSP00000221421.1:p.Pro112His
ENST00000391869.4:c.329C>A	ENSP00000375742.4:p.Pro110His
NM_000894.2:c.335C>A	NP_000885.1:p.Pro112His
XM_011526975.1:c.383C>A	XP_011525277.1:p.Pro128His
NM_000894.3:c.335C>A MANE Select	NP_000885.1:p.Pro112His