Canonical Allele Identifier: CA863718723

Gene: GRHPR

Linked Data

• dbSNP Id: rs1171280908
• gnomAD v4: 9-37429682-C-T
• MyVariant Identifiers: chr9:g.37429679C>T (hg19) ; chr9:g.37429682C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429682C>T , CM000671.2:g.37429682C>T	GRCh38
NC_000009.11:g.37429679C>T , CM000671.1:g.37429679C>T	GRCh37
NC_000009.10:g.37419679C>T	NCBI36
NG_008135.1:g.11973C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-50C>T MANE Select	ENSP00000313432.6:n.494-50C>T
ENST00000318158.10:c.494-50C>T	ENSP00000313432.6:n.494-50C>T
ENST00000377824.8:n.531-50C>T
ENST00000460882.5:n.521-50C>T
ENST00000480596.5:n.1145C>T
ENST00000491488.5:n.199-50C>T
ENST00000494290.1:c.15C>T	ENSP00000432021.1:p.Val5=
ENST00000497693.1:n.1977C>T
ENST00000607784.1:c.494-50C>T	ENSP00000475569.1:n.494-50C>T
NM_012203.1:c.494-50C>T	NP_036335.1:n.494-50C>T
XM_005251631.1:c.173-50C>T	XP_005251688.1:n.173-50C>T
XM_011518073.1:c.92-50C>T	XP_011516375.1:n.92-50C>T
XR_929374.1:n.939-50C>T
XM_017015320.2:c.494-50C>T	XP_016870809.1:n.494-50C>T
XM_017015321.2:c.494-50C>T	XP_016870810.1:n.494-50C>T
XM_017015323.2:c.92-50C>T	XP_016870812.1:n.92-50C>T
XM_024447716.1:c.767-50C>T	XP_024303484.1:n.767-50C>T
XM_024447717.1:c.767-50C>T	XP_024303485.1:n.767-50C>T
XR_002956828.1:n.782-50C>T
XR_002956829.1:n.782-50C>T
XR_002956830.1:n.553-50C>T
XR_002956831.1:n.228-50C>T
XR_002956832.1:n.913-50C>T
NM_012203.2:c.494-50C>T MANE Select	NP_036335.1:n.494-50C>T