Canonical Allele Identifier: CA406776369
Gene: LHB HGNC NCBI

Linked Data

dbSNP Id: rs2122671009
MyVariant Identifiers: chr19:g.49519366T>C (hg19) chr19:g.49016109T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016109T>C , CM000681.2:g.49016109T>C GRCh38
NC_000019.9:g.49519366T>C , CM000681.1:g.49519366T>C GRCh37
NC_000019.8:g.54211178T>C NCBI36
NG_011464.1:g.5982A>G
NG_033041.1:g.27211T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649238.3:c.385A>G MANE Select ENSP00000497294.2:p.Thr129Ala
ENST00000649284.1:n.476A>G
ENST00000221421.6:c.385A>G ENSP00000221421.1:p.Thr129Ala
ENST00000391869.4:c.379A>G ENSP00000375742.4:p.Thr127Ala
NM_000894.2:c.385A>G NP_000885.1:p.Thr129Ala
XM_011526975.1:c.433A>G XP_011525277.1:p.Thr145Ala
NM_000894.3:c.385A>G MANE Select NP_000885.1:p.Thr129Ala
Search 100 bp 5'
Search 100 bp 3'