Canonical Allele Identifier: CA2586297823

Gene: LHB

Linked Data

• gnomAD v4: 19-49016012-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49016012C>A , CM000681.2:g.49016012C>A	GRCh38
NC_000019.9:g.49519269C>A , CM000681.1:g.49519269C>A	GRCh37
NC_000019.8:g.54211081C>A	NCBI36
NG_011464.1:g.6079G>T
NG_033041.1:g.27114C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649238.3:c.*56G>T MANE Select	ENSP00000497294.2:n.*56G>T
ENST00000221421.6:c.482G>T	ENSP00000221421.1:n.482G>T
NM_000894.2:c.*56G>T	NP_000885.1:n.*56G>T
XM_011526975.1:c.*56G>T	XP_011525277.1:n.*56G>T
NM_000894.3:c.*56G>T MANE Select	NP_000885.1:n.*56G>T