Canonical Allele Identifier: CA406777051
Gene: LHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49519372G>A (hg19) chr19:g.49016115G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016115G>A , CM000681.2:g.49016115G>A GRCh38
NC_000019.9:g.49519372G>A , CM000681.1:g.49519372G>A GRCh37
NC_000019.8:g.54211184G>A NCBI36
NG_011464.1:g.5976C>T
NG_033041.1:g.27217G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649238.3:c.379C>T MANE Select ENSP00000497294.2:p.Pro127Ser
ENST00000649284.1:n.470C>T
ENST00000221421.6:c.379C>T ENSP00000221421.1:p.Pro127Ser
ENST00000391869.4:c.373C>T ENSP00000375742.4:p.Pro125Ser
NM_000894.2:c.379C>T NP_000885.1:p.Pro127Ser
XM_011526975.1:c.427C>T XP_011525277.1:p.Pro143Ser
NM_000894.3:c.379C>T MANE Select NP_000885.1:p.Pro127Ser
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