Canonical Allele Identifier: CA1846886888

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823695783
• gnomAD v4: 9-37436920-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436920C>T , CM000671.2:g.37436920C>T	GRCh38
NC_000009.11:g.37436917C>T , CM000671.1:g.37436917C>T	GRCh37
NC_000009.10:g.37426917C>T	NCBI36
NG_008135.1:g.19211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*138C>T MANE Select	ENSP00000313432.6:n.*138C>T
ENST00000318158.10:c.*138C>T	ENSP00000313432.6:n.*138C>T
ENST00000480596.5:n.1826C>T
ENST00000494290.1:c.*91C>T	ENSP00000432021.1:n.*91C>T
ENST00000497693.1:n.4693C>T
NM_012203.1:c.*138C>T	NP_036335.1:n.*138C>T
XM_005251631.1:c.*138C>T	XP_005251688.1:n.*138C>T
XM_011518073.1:c.*138C>T	XP_011516375.1:n.*138C>T
XM_017015320.2:c.946-491C>T	XP_016870809.1:n.946-491C>T
XM_017015321.2:c.866-491C>T	XP_016870810.1:n.866-491C>T
XM_017015323.2:c.544-491C>T	XP_016870812.1:n.544-491C>T
XM_024447716.1:c.1219-491C>T	XP_024303484.1:n.1219-491C>T
XM_024447717.1:c.1139-491C>T	XP_024303485.1:n.1139-491C>T
XR_002956828.1:n.1234-491C>T
XR_002956829.1:n.1154-491C>T
XR_002956830.1:n.2545C>T
XR_002956831.1:n.2220C>T
XR_002956832.1:n.1544C>T
NM_012203.2:c.*138C>T MANE Select	NP_036335.1:n.*138C>T