Canonical Allele Identifier: CA2739624276
Gene: LHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016010A>T , CM000681.2:g.49016010A>T GRCh38
NC_000019.9:g.49519267A>T , CM000681.1:g.49519267A>T GRCh37
NC_000019.8:g.54211079A>T NCBI36
NG_011464.1:g.6081T>A
NG_033041.1:g.27112A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.*58T>A MANE Select ENSP00000497294.2:n.*58T>A
ENST00000221421.6:c.484T>A ENSP00000221421.1:n.484T>A
NM_000894.2:c.*58T>A NP_000885.1:n.*58T>A
XM_011526975.1:c.*58T>A XP_011525277.1:n.*58T>A
NM_000894.3:c.*58T>A MANE Select NP_000885.1:n.*58T>A
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