Canonical Allele Identifier: CA406776357
Gene: LHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49519365G>C (hg19) chr19:g.49016108G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016108G>C , CM000681.2:g.49016108G>C GRCh38
NC_000019.9:g.49519365G>C , CM000681.1:g.49519365G>C GRCh37
NC_000019.8:g.54211177G>C NCBI36
NG_011464.1:g.5983C>G
NG_033041.1:g.27210G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.386C>G MANE Select ENSP00000497294.2:p.Thr129Ser
ENST00000649284.1:n.477C>G
ENST00000221421.6:c.386C>G ENSP00000221421.1:p.Thr129Ser
ENST00000391869.4:c.380C>G ENSP00000375742.4:p.Thr127Ser
NM_000894.2:c.386C>G NP_000885.1:p.Thr129Ser
XM_011526975.1:c.434C>G XP_011525277.1:p.Thr145Ser
NM_000894.3:c.386C>G MANE Select NP_000885.1:p.Thr129Ser
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