Canonical Allele Identifier: CA508277296

Gene: LHB

Linked Data

• gnomAD v4: 19-49016206-C-T
• MyVariant Identifiers: chr19:g.49519463C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016206C>T , CM000681.2:g.49016206C>T	GRCh38
NC_000019.9:g.49519463C>T , CM000681.1:g.49519463C>T	GRCh37
NC_000019.8:g.54211275C>T	NCBI36
NG_011464.1:g.5885G>A
NG_033041.1:g.27308C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.288G>A MANE Select	ENSP00000497294.2:p.Val96=
ENST00000649284.1:n.379G>A
ENST00000221421.6:c.288G>A	ENSP00000221421.1:p.Val96=
ENST00000391869.4:c.282G>A	ENSP00000375742.4:p.Val94=
NM_000894.2:c.288G>A	NP_000885.1:p.Val96=
XM_011526975.1:c.336G>A	XP_011525277.1:p.Val112=
NM_000894.3:c.288G>A MANE Select	NP_000885.1:p.Val96=