Canonical Allele Identifier: CA373442119

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37425933G>T (hg19) ; chr9:g.37425936G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425936G>T , CM000671.2:g.37425936G>T	GRCh38
NC_000009.11:g.37425933G>T , CM000671.1:g.37425933G>T	GRCh37
NC_000009.10:g.37415933G>T	NCBI36
NG_008135.1:g.8227G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.229G>T MANE Select	ENSP00000313432.6:p.Val77Phe
ENST00000318158.10:c.229G>T	ENSP00000313432.6:p.Val77Phe
ENST00000377824.8:n.266G>T
ENST00000460882.5:n.256G>T
ENST00000487399.5:n.238G>T
ENST00000491488.5:n.110-2548G>T
ENST00000493368.5:n.286G>T
ENST00000607784.1:c.229G>T	ENSP00000475569.1:p.Val77Phe
NM_012203.1:c.229G>T	NP_036335.1:p.Val77Phe
XM_005251631.1:c.84-2548G>T	XP_005251688.1:n.84-2548G>T
XM_011518073.1:c.-534G>T	XP_011516375.1:n.-534G>T
XR_929374.1:n.314G>T
XM_017015320.2:c.229G>T	XP_016870809.1:p.Val77Phe
XM_017015321.2:c.229G>T	XP_016870810.1:p.Val77Phe
XM_017015323.2:c.-534G>T	XP_016870812.1:n.-534G>T
XM_024447716.1:c.502G>T	XP_024303484.1:p.Val168Phe
XM_024447717.1:c.502G>T	XP_024303485.1:p.Val168Phe
XR_002956828.1:n.517G>T
XR_002956829.1:n.517G>T
XR_002956830.1:n.288G>T
XR_002956831.1:n.139-2548G>T
XR_002956832.1:n.288G>T
NM_012203.2:c.229G>T MANE Select	NP_036335.1:p.Val77Phe