Canonical Allele Identifier: CA373442412

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37426537G>T (hg19) ; chr9:g.37426540G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426540G>T , CM000671.2:g.37426540G>T	GRCh38
NC_000009.11:g.37426537G>T , CM000671.1:g.37426537G>T	GRCh37
NC_000009.10:g.37416537G>T	NCBI36
NG_008135.1:g.8831G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.290G>T MANE Select	ENSP00000313432.6:p.Gly97Val
ENST00000318158.10:c.290G>T	ENSP00000313432.6:p.Gly97Val
ENST00000377824.8:n.327G>T
ENST00000460882.5:n.317G>T
ENST00000487399.5:n.842G>T
ENST00000491488.5:n.110-1944G>T
ENST00000493368.5:n.347G>T
ENST00000607784.1:c.290G>T	ENSP00000475569.1:p.Gly97Val
NM_012203.1:c.290G>T	NP_036335.1:p.Gly97Val
XM_005251631.1:c.84-1944G>T	XP_005251688.1:n.84-1944G>T
XM_011518073.1:c.-473G>T	XP_011516375.1:n.-473G>T
XR_929374.1:n.375G>T
XM_017015320.2:c.290G>T	XP_016870809.1:p.Gly97Val
XM_017015321.2:c.290G>T	XP_016870810.1:p.Gly97Val
XM_017015323.2:c.-473G>T	XP_016870812.1:n.-473G>T
XM_024447716.1:c.563G>T	XP_024303484.1:p.Gly188Val
XM_024447717.1:c.563G>T	XP_024303485.1:p.Gly188Val
XR_002956828.1:n.578G>T
XR_002956829.1:n.578G>T
XR_002956830.1:n.349G>T
XR_002956831.1:n.139-1944G>T
XR_002956832.1:n.349G>T
NM_012203.2:c.290G>T MANE Select	NP_036335.1:p.Gly97Val