Canonical Allele Identifier: CA2340186941
Gene: LHB HGNC NCBI

Linked Data

dbSNP Id: rs780562920
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016009G>T , CM000681.2:g.49016009G>T GRCh38
NC_000019.9:g.49519266G>T , CM000681.1:g.49519266G>T GRCh37
NC_000019.8:g.54211078G>T NCBI36
NG_011464.1:g.6082C>A
NG_033041.1:g.27111G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.*59C>A MANE Select ENSP00000497294.2:n.*59C>A
ENST00000221421.6:c.485C>A ENSP00000221421.1:n.485C>A
NM_000894.2:c.*59C>A NP_000885.1:n.*59C>A
XM_011526975.1:c.*59C>A XP_011525277.1:n.*59C>A
NM_000894.3:c.*59C>A MANE Select NP_000885.1:n.*59C>A
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