Canonical Allele Identifier: CA406777064
Gene: LHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49519374T>G (hg19) chr19:g.49016117T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49016117T>G , CM000681.2:g.49016117T>G GRCh38
NC_000019.9:g.49519374T>G , CM000681.1:g.49519374T>G GRCh37
NC_000019.8:g.54211186T>G NCBI36
NG_011464.1:g.5974A>C
NG_033041.1:g.27219T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649238.3:c.377A>C MANE Select ENSP00000497294.2:p.His126Pro
ENST00000649284.1:n.468A>C
ENST00000221421.6:c.377A>C ENSP00000221421.1:p.His126Pro
ENST00000391869.4:c.371A>C ENSP00000375742.4:p.His124Pro
NM_000894.2:c.377A>C NP_000885.1:p.His126Pro
XM_011526975.1:c.425A>C XP_011525277.1:p.His142Pro
NM_000894.3:c.377A>C MANE Select NP_000885.1:p.His126Pro
Search 100 bp 5'
Search 100 bp 3'