Canonical Allele Identifier: CA406777048
Gene: LHB HGNC NCBI

Linked Data

dbSNP Id: rs2039546039
MyVariant Identifiers: chr19:g.49519371G>C (hg19) chr19:g.49016114G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016114G>C , CM000681.2:g.49016114G>C GRCh38
NC_000019.9:g.49519371G>C , CM000681.1:g.49519371G>C GRCh37
NC_000019.8:g.54211183G>C NCBI36
NG_011464.1:g.5977C>G
NG_033041.1:g.27216G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649238.3:c.380C>G MANE Select ENSP00000497294.2:p.Pro127Arg
ENST00000649284.1:n.471C>G
ENST00000221421.6:c.380C>G ENSP00000221421.1:p.Pro127Arg
ENST00000391869.4:c.374C>G ENSP00000375742.4:p.Pro125Arg
NM_000894.2:c.380C>G NP_000885.1:p.Pro127Arg
XM_011526975.1:c.428C>G XP_011525277.1:p.Pro143Arg
NM_000894.3:c.380C>G MANE Select NP_000885.1:p.Pro127Arg
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