Canonical Allele Identifier: CA406777351
Gene: LHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49519464A>C (hg19) chr19:g.49016207A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016207A>C , CM000681.2:g.49016207A>C GRCh38
NC_000019.9:g.49519464A>C , CM000681.1:g.49519464A>C GRCh37
NC_000019.8:g.54211276A>C NCBI36
NG_011464.1:g.5884T>G
NG_033041.1:g.27309A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649238.3:c.287T>G MANE Select ENSP00000497294.2:p.Val96Gly
ENST00000649284.1:n.378T>G
ENST00000221421.6:c.287T>G ENSP00000221421.1:p.Val96Gly
ENST00000391869.4:c.281T>G ENSP00000375742.4:p.Val94Gly
NM_000894.2:c.287T>G NP_000885.1:p.Val96Gly
XM_011526975.1:c.335T>G XP_011525277.1:p.Val112Gly
NM_000894.3:c.287T>G MANE Select NP_000885.1:p.Val96Gly
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