Canonical Allele Identifier: CA465003981

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428529-A-G
• MyVariant Identifiers: chr9:g.37428526A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428529A>G , CM000671.2:g.37428529A>G	GRCh38
NC_000009.11:g.37428526A>G , CM000671.1:g.37428526A>G	GRCh37
NC_000009.10:g.37418526A>G	NCBI36
NG_008135.1:g.10820A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.450A>G MANE Select	ENSP00000313432.6:p.Gly150=
ENST00000318158.10:c.450A>G	ENSP00000313432.6:p.Gly150=
ENST00000377824.8:n.487A>G
ENST00000460882.5:n.477A>G
ENST00000491488.5:n.155A>G
ENST00000493368.5:n.507A>G
ENST00000497693.1:n.824A>G
ENST00000607784.1:c.450A>G	ENSP00000475569.1:p.Gly150=
NM_012203.1:c.450A>G	NP_036335.1:p.Gly150=
XM_005251631.1:c.129A>G	XP_005251688.1:p.Gly43=
XM_011518073.1:c.-313A>G	XP_011516375.1:n.-313A>G
XR_929374.1:n.535A>G
XM_017015320.2:c.450A>G	XP_016870809.1:p.Gly150=
XM_017015321.2:c.450A>G	XP_016870810.1:p.Gly150=
XM_017015323.2:c.-313A>G	XP_016870812.1:n.-313A>G
XM_024447716.1:c.723A>G	XP_024303484.1:p.Gly241=
XM_024447717.1:c.723A>G	XP_024303485.1:p.Gly241=
XR_002956828.1:n.738A>G
XR_002956829.1:n.738A>G
XR_002956830.1:n.509A>G
XR_002956831.1:n.184A>G
XR_002956832.1:n.509A>G
NM_012203.2:c.450A>G MANE Select	NP_036335.1:p.Gly150=