Canonical Allele Identifier: CA508277278

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519442A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016185A>C , CM000681.2:g.49016185A>C	GRCh38
NC_000019.9:g.49519442A>C , CM000681.1:g.49519442A>C	GRCh37
NC_000019.8:g.54211254A>C	NCBI36
NG_011464.1:g.5906T>G
NG_033041.1:g.27287A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.309T>G MANE Select	ENSP00000497294.2:p.Pro103=
ENST00000649284.1:n.400T>G
ENST00000221421.6:c.309T>G	ENSP00000221421.1:p.Pro103=
ENST00000391869.4:c.303T>G	ENSP00000375742.4:p.Pro101=
NM_000894.2:c.309T>G	NP_000885.1:p.Pro103=
XM_011526975.1:c.357T>G	XP_011525277.1:p.Pro119=
NM_000894.3:c.309T>G MANE Select	NP_000885.1:p.Pro103=