Canonical Allele Identifier: CA3254415
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1400686
ClinVar RCV Id: RCV001911442
dbSNP Id: rs745367760
gnomAD v2: 5-42699944-T-C
gnomAD v3: 5-42699842-T-C
gnomAD v4: 5-42699842-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.42699842T>C , CM000667.2:g.42699842T>C GRCh38
NC_000005.9:g.42699944T>C , CM000667.1:g.42699944T>C GRCh37
NC_000005.8:g.42735701T>C NCBI36
NG_011688.1:g.280919T>C
NG_011688.2:g.280919T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000230882.9:c.458T>C MANE Select ENSP00000230882.4:p.Ile153Thr
ENST00000230882.8:c.458T>C ENSP00000230882.4:p.Ile153Thr
ENST00000357703.6:c.392T>C ENSP00000350335.3:p.Ile131Thr
ENST00000511135.5:c.*70T>C ENSP00000422333.1:n.*70T>C
ENST00000537449.5:c.458T>C ENSP00000442206.2:p.Ile153Thr
ENST00000612382.4:c.458T>C ENSP00000478332.1:p.Ile153Thr
ENST00000612626.4:c.458T>C ENSP00000479846.1:p.Ile153Thr
ENST00000615111.4:c.458T>C ENSP00000478291.1:p.Ile153Thr
ENST00000618088.4:c.458T>C ENSP00000482373.1:p.Ile153Thr
ENST00000620156.4:c.479T>C ENSP00000483403.1:p.Ile160Thr
ENST00000622294.2:c.458T>C ENSP00000483926.1:p.Ile153Thr
NM_000163.4:c.458T>C NP_000154.1:p.Ile153Thr
NM_001242399.2:c.479T>C NP_001229328.1:p.Ile160Thr
NM_001242400.2:c.458T>C NP_001229329.1:p.Ile153Thr
NM_001242401.3:c.458T>C NP_001229330.1:p.Ile153Thr
NM_001242402.2:c.458T>C NP_001229331.1:p.Ile153Thr
NM_001242403.2:c.458T>C NP_001229332.1:p.Ile153Thr
NM_001242404.2:c.458T>C NP_001229333.1:p.Ile153Thr
NM_001242405.2:c.458T>C NP_001229334.1:p.Ile153Thr
NM_001242406.2:c.458T>C NP_001229335.1:p.Ile153Thr
NM_001242460.1:c.392T>C NP_001229389.1:p.Ile131Thr
NM_001242462.1:c.458T>C NP_001229391.1:p.Ile153Thr
XM_011514031.1:c.413T>C XP_011512333.1:p.Ile138Thr
NM_000163.5:c.458T>C MANE Select NP_000154.1:p.Ile153Thr
NM_001242401.4:c.458T>C NP_001229330.1:p.Ile153Thr
NM_001242403.3:c.458T>C NP_001229332.1:p.Ile153Thr