Canonical Allele Identifier: CA465006866

Gene: GRHPR

Linked Data

• dbSNP Id: rs2098382135
• MyVariant Identifiers: chr9:g.37436749G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436752G>A , CM000671.2:g.37436752G>A	GRCh38
NC_000009.11:g.37436749G>A , CM000671.1:g.37436749G>A	GRCh37
NC_000009.10:g.37426749G>A	NCBI36
NG_008135.1:g.19043G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.957G>A MANE Select	ENSP00000313432.6:p.Gly319=
ENST00000318158.10:c.957G>A	ENSP00000313432.6:p.Gly319=
ENST00000460882.5:n.984G>A
ENST00000480596.5:n.1658G>A
ENST00000494290.1:c.*52-129G>A	ENSP00000432021.1:n.*52-129G>A
ENST00000497693.1:n.4525G>A
NM_012203.1:c.957G>A	NP_036335.1:p.Gly319=
XM_005251631.1:c.636G>A	XP_005251688.1:p.Gly212=
XM_011518073.1:c.555G>A	XP_011516375.1:p.Gly185=
XM_017015320.2:c.946-659G>A	XP_016870809.1:n.946-659G>A
XM_017015321.2:c.866-659G>A	XP_016870810.1:n.866-659G>A
XM_017015323.2:c.544-659G>A	XP_016870812.1:n.544-659G>A
XM_024447716.1:c.1219-659G>A	XP_024303484.1:n.1219-659G>A
XM_024447717.1:c.1139-659G>A	XP_024303485.1:n.1139-659G>A
XR_002956828.1:n.1234-659G>A
XR_002956829.1:n.1154-659G>A
XR_002956830.1:n.2377G>A
XR_002956831.1:n.2052G>A
XR_002956832.1:n.1376G>A
NM_012203.2:c.957G>A MANE Select	NP_036335.1:p.Gly319=