Canonical Allele Identifier: CA5059073

Gene: GRHPR

Linked Data

• dbSNP Id: rs374838995
• ExAC: 9:37428597 G / A
• gnomAD v2: 9-37428597-G-A
• gnomAD v3: 9-37428600-G-A
• gnomAD v4: 9-37428600-G-A
• MyVariant Identifiers: chr9:g.37428597G>A (hg19) ; chr9:g.37428600G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428600G>A , CM000671.2:g.37428600G>A	GRCh38
NC_000009.11:g.37428597G>A , CM000671.1:g.37428597G>A	GRCh37
NC_000009.10:g.37418597G>A	NCBI36
NG_008135.1:g.10891G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+28G>A MANE Select	ENSP00000313432.6:n.493+28G>A
ENST00000318158.10:c.493+28G>A	ENSP00000313432.6:n.493+28G>A
ENST00000377824.8:n.530+28G>A
ENST00000460882.5:n.520+28G>A
ENST00000480596.5:n.63G>A
ENST00000491488.5:n.198+28G>A
ENST00000493368.5:n.578G>A
ENST00000497693.1:n.895G>A
ENST00000607784.1:c.493+28G>A	ENSP00000475569.1:n.493+28G>A
NM_012203.1:c.493+28G>A	NP_036335.1:n.493+28G>A
XM_005251631.1:c.172+28G>A	XP_005251688.1:n.172+28G>A
XM_011518073.1:c.-242G>A	XP_011516375.1:n.-242G>A
XR_929374.1:n.606G>A
XM_017015320.2:c.493+28G>A	XP_016870809.1:n.493+28G>A
XM_017015321.2:c.493+28G>A	XP_016870810.1:n.493+28G>A
XM_017015323.2:c.-242G>A	XP_016870812.1:n.-242G>A
XM_024447716.1:c.766+28G>A	XP_024303484.1:n.766+28G>A
XM_024447717.1:c.766+28G>A	XP_024303485.1:n.766+28G>A
XR_002956828.1:n.781+28G>A
XR_002956829.1:n.781+28G>A
XR_002956830.1:n.552+28G>A
XR_002956831.1:n.227+28G>A
XR_002956832.1:n.580G>A
NM_012203.2:c.493+28G>A MANE Select	NP_036335.1:n.493+28G>A