Canonical Allele Identifier: CA558917312
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1996427
ClinVar RCV Id: RCV002802047
dbSNP Id: rs1324055633
gnomAD v2: 5-42695204-T-G
gnomAD v4: 5-42695102-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.42695102T>G , CM000667.2:g.42695102T>G GRCh38
NC_000005.9:g.42695204T>G , CM000667.1:g.42695204T>G GRCh37
NC_000005.8:g.42730961T>G NCBI36
NG_011688.1:g.276179T>G
NG_011688.2:g.276179T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000230882.9:c.439+13T>G MANE Select ENSP00000230882.4:n.439+13T>G
ENST00000230882.8:c.439+13T>G ENSP00000230882.4:n.439+13T>G
ENST00000357703.6:c.373+13T>G ENSP00000350335.3:n.373+13T>G
ENST00000511135.5:c.*51+13T>G ENSP00000422333.1:n.*51+13T>G
ENST00000537449.5:c.439+13T>G ENSP00000442206.2:n.439+13T>G
ENST00000612382.4:c.439+13T>G ENSP00000478332.1:n.439+13T>G
ENST00000612626.4:c.439+13T>G ENSP00000479846.1:n.439+13T>G
ENST00000615111.4:c.439+13T>G ENSP00000478291.1:n.439+13T>G
ENST00000618088.4:c.439+13T>G ENSP00000482373.1:n.439+13T>G
ENST00000620156.4:c.460+13T>G ENSP00000483403.1:n.460+13T>G
ENST00000622294.2:c.439+13T>G ENSP00000483926.1:n.439+13T>G
NM_000163.4:c.439+13T>G NP_000154.1:n.439+13T>G
NM_001242399.2:c.460+13T>G NP_001229328.1:n.460+13T>G
NM_001242400.2:c.439+13T>G NP_001229329.1:n.439+13T>G
NM_001242401.3:c.439+13T>G NP_001229330.1:n.439+13T>G
NM_001242402.2:c.439+13T>G NP_001229331.1:n.439+13T>G
NM_001242403.2:c.439+13T>G NP_001229332.1:n.439+13T>G
NM_001242404.2:c.439+13T>G NP_001229333.1:n.439+13T>G
NM_001242405.2:c.439+13T>G NP_001229334.1:n.439+13T>G
NM_001242406.2:c.439+13T>G NP_001229335.1:n.439+13T>G
NM_001242460.1:c.373+13T>G NP_001229389.1:n.373+13T>G
NM_001242462.1:c.439+13T>G NP_001229391.1:n.439+13T>G
XM_011514031.1:c.394+13T>G XP_011512333.1:n.394+13T>G
NM_000163.5:c.439+13T>G MANE Select NP_000154.1:n.439+13T>G
NM_001242401.4:c.439+13T>G NP_001229330.1:n.439+13T>G
NM_001242403.3:c.439+13T>G NP_001229332.1:n.439+13T>G