Canonical Allele Identifier: CA406777209

Gene: LHB

Linked Data

• MyVariant Identifiers: chr19:g.49519413C>G (hg19) ; chr19:g.49016156C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016156C>G , CM000681.2:g.49016156C>G	GRCh38
NC_000019.9:g.49519413C>G , CM000681.1:g.49519413C>G	GRCh37
NC_000019.8:g.54211225C>G	NCBI36
NG_011464.1:g.5935G>C
NG_033041.1:g.27258C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.338G>C MANE Select	ENSP00000497294.2:p.Cys113Ser
ENST00000649284.1:n.429G>C
ENST00000221421.6:c.338G>C	ENSP00000221421.1:p.Cys113Ser
ENST00000391869.4:c.332G>C	ENSP00000375742.4:p.Cys111Ser
NM_000894.2:c.338G>C	NP_000885.1:p.Cys113Ser
XM_011526975.1:c.386G>C	XP_011525277.1:p.Cys129Ser
NM_000894.3:c.338G>C MANE Select	NP_000885.1:p.Cys113Ser