Canonical Allele Identifier: CA508277255
Gene: LHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49519406G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016149G>C , CM000681.2:g.49016149G>C GRCh38
NC_000019.9:g.49519406G>C , CM000681.1:g.49519406G>C GRCh37
NC_000019.8:g.54211218G>C NCBI36
NG_011464.1:g.5942C>G
NG_033041.1:g.27251G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.345C>G MANE Select ENSP00000497294.2:p.Arg115=
ENST00000649284.1:n.436C>G
ENST00000221421.6:c.345C>G ENSP00000221421.1:p.Arg115=
ENST00000391869.4:c.339C>G ENSP00000375742.4:p.Arg113=
NM_000894.2:c.345C>G NP_000885.1:p.Arg115=
XM_011526975.1:c.393C>G XP_011525277.1:p.Arg131=
NM_000894.3:c.345C>G MANE Select NP_000885.1:p.Arg115=
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