Canonical Allele Identifier: CA373441513

Gene: GRHPR

Linked Data

• ClinVar Variation Id: 2340723
• ClinVar RCV Id: RCV004187530
• dbSNP Id: rs150805048
• MyVariant Identifiers: chr9:g.37424907C>G (hg19) ; chr9:g.37424910C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424910C>G , CM000671.2:g.37424910C>G	GRCh38
NC_000009.11:g.37424907C>G , CM000671.1:g.37424907C>G	GRCh37
NC_000009.10:g.37414907C>G	NCBI36
NG_008135.1:g.7201C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.149C>G MANE Select	ENSP00000313432.6:p.Ala50Gly
ENST00000318158.10:c.149C>G	ENSP00000313432.6:p.Ala50Gly
ENST00000377824.8:n.186C>G
ENST00000460882.5:n.176C>G
ENST00000487399.5:n.158C>G
ENST00000491488.5:n.109+2077C>G
ENST00000493368.5:n.206C>G
ENST00000607784.1:c.149C>G	ENSP00000475569.1:p.Ala50Gly
NM_012203.1:c.149C>G	NP_036335.1:p.Ala50Gly
XM_005251631.1:c.83+2077C>G	XP_005251688.1:n.83+2077C>G
XM_011518073.1:c.-614C>G	XP_011516375.1:n.-614C>G
XR_929374.1:n.234C>G
XM_017015320.2:c.149C>G	XP_016870809.1:p.Ala50Gly
XM_017015321.2:c.149C>G	XP_016870810.1:p.Ala50Gly
XM_017015323.2:c.-614C>G	XP_016870812.1:n.-614C>G
XM_024447716.1:c.422C>G	XP_024303484.1:p.Ala141Gly
XM_024447717.1:c.422C>G	XP_024303485.1:p.Ala141Gly
XR_002956828.1:n.437C>G
XR_002956829.1:n.437C>G
XR_002956830.1:n.208C>G
XR_002956831.1:n.138+2077C>G
XR_002956832.1:n.208C>G
NM_012203.2:c.149C>G MANE Select	NP_036335.1:p.Ala50Gly