Canonical Allele Identifier: CA3254355

Gene: GHR

Linked Data

• ClinVar Variation Id: 449369
• ClinVar RCV Id: RCV000522157
• dbSNP Id: rs114025919
• ExAC: 5:42689094 G / T
• gnomAD v2: 5-42689094-G-T
• gnomAD v3: 5-42688992-G-T
• gnomAD v4: 5-42688992-G-T
• MyVariant Identifiers: chr5:g.42689094G>T (hg19) ; chr5:g.42688992G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42688992G>T , CM000667.2:g.42688992G>T	GRCh38
NC_000005.9:g.42689094G>T , CM000667.1:g.42689094G>T	GRCh37
NC_000005.8:g.42724851G>T	NCBI36
NG_011688.1:g.270069G>T
NG_011688.2:g.270069G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230882.9:c.239G>T MANE Select	ENSP00000230882.4:p.Gly80Val
ENST00000230882.8:c.239G>T	ENSP00000230882.4:p.Gly80Val
ENST00000357703.6:c.173G>T	ENSP00000350335.3:p.Gly58Val
ENST00000511135.5:c.137-5925G>T	ENSP00000422333.1:n.137-5925G>T
ENST00000537449.5:c.239G>T	ENSP00000442206.2:p.Gly80Val
ENST00000612382.4:c.239G>T	ENSP00000478332.1:p.Gly80Val
ENST00000612626.4:c.239G>T	ENSP00000479846.1:p.Gly80Val
ENST00000615111.4:c.239G>T	ENSP00000478291.1:p.Gly80Val
ENST00000618088.4:c.239G>T	ENSP00000482373.1:p.Gly80Val
ENST00000620156.4:c.260G>T	ENSP00000483403.1:p.Gly87Val
ENST00000622294.2:c.239G>T	ENSP00000483926.1:p.Gly80Val
NM_000163.4:c.239G>T	NP_000154.1:p.Gly80Val
NM_001242399.2:c.260G>T	NP_001229328.1:p.Gly87Val
NM_001242400.2:c.239G>T	NP_001229329.1:p.Gly80Val
NM_001242401.3:c.239G>T	NP_001229330.1:p.Gly80Val
NM_001242402.2:c.239G>T	NP_001229331.1:p.Gly80Val
NM_001242403.2:c.239G>T	NP_001229332.1:p.Gly80Val
NM_001242404.2:c.239G>T	NP_001229333.1:p.Gly80Val
NM_001242405.2:c.239G>T	NP_001229334.1:p.Gly80Val
NM_001242406.2:c.239G>T	NP_001229335.1:p.Gly80Val
NM_001242460.1:c.173G>T	NP_001229389.1:p.Gly58Val
NM_001242462.1:c.239G>T	NP_001229391.1:p.Gly80Val
XM_011514031.1:c.194G>T	XP_011512333.1:p.Gly65Val
NM_000163.5:c.239G>T MANE Select	NP_000154.1:p.Gly80Val
NM_001242401.4:c.239G>T	NP_001229330.1:p.Gly80Val
NM_001242403.3:c.239G>T	NP_001229332.1:p.Gly80Val