Canonical Allele Identifier: CA192890384

Gene: GRHPR

Linked Data

• dbSNP Id: rs539810600
• gnomAD v2: 9-37429654-C-A
• gnomAD v4: 9-37429657-C-A
• MyVariant Identifiers: chr9:g.37429654C>A (hg19) ; chr9:g.37429657C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429657C>A , CM000671.2:g.37429657C>A	GRCh38
NC_000009.11:g.37429654C>A , CM000671.1:g.37429654C>A	GRCh37
NC_000009.10:g.37419654C>A	NCBI36
NG_008135.1:g.11948C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-75C>A MANE Select	ENSP00000313432.6:n.494-75C>A
ENST00000318158.10:c.494-75C>A	ENSP00000313432.6:n.494-75C>A
ENST00000377824.8:n.531-75C>A
ENST00000460882.5:n.521-75C>A
ENST00000480596.5:n.1120C>A
ENST00000491488.5:n.199-75C>A
ENST00000494290.1:c.-11C>A	ENSP00000432021.1:n.-11C>A
ENST00000497693.1:n.1952C>A
ENST00000607784.1:c.494-75C>A	ENSP00000475569.1:n.494-75C>A
NM_012203.1:c.494-75C>A	NP_036335.1:n.494-75C>A
XM_005251631.1:c.173-75C>A	XP_005251688.1:n.173-75C>A
XM_011518073.1:c.92-75C>A	XP_011516375.1:n.92-75C>A
XR_929374.1:n.939-75C>A
XM_017015320.2:c.494-75C>A	XP_016870809.1:n.494-75C>A
XM_017015321.2:c.494-75C>A	XP_016870810.1:n.494-75C>A
XM_017015323.2:c.92-75C>A	XP_016870812.1:n.92-75C>A
XM_024447716.1:c.767-75C>A	XP_024303484.1:n.767-75C>A
XM_024447717.1:c.767-75C>A	XP_024303485.1:n.767-75C>A
XR_002956828.1:n.782-75C>A
XR_002956829.1:n.782-75C>A
XR_002956830.1:n.553-75C>A
XR_002956831.1:n.228-75C>A
XR_002956832.1:n.913-75C>A
NM_012203.2:c.494-75C>A MANE Select	NP_036335.1:n.494-75C>A