Canonical Allele Identifier: CA508277213
Gene: LHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49519370G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016113G>T , CM000681.2:g.49016113G>T GRCh38
NC_000019.9:g.49519370G>T , CM000681.1:g.49519370G>T GRCh37
NC_000019.8:g.54211182G>T NCBI36
NG_011464.1:g.5978C>A
NG_033041.1:g.27215G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649238.3:c.381C>A MANE Select ENSP00000497294.2:p.Pro127=
ENST00000649284.1:n.472C>A
ENST00000221421.6:c.381C>A ENSP00000221421.1:p.Pro127=
ENST00000391869.4:c.375C>A ENSP00000375742.4:p.Pro125=
NM_000894.2:c.381C>A NP_000885.1:p.Pro127=
XM_011526975.1:c.429C>A XP_011525277.1:p.Pro143=
NM_000894.3:c.381C>A MANE Select NP_000885.1:p.Pro127=
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