Canonical Allele Identifier: CA2689984714

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436958-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436958A>G , CM000671.2:g.37436958A>G	GRCh38
NC_000009.11:g.37436955A>G , CM000671.1:g.37436955A>G	GRCh37
NC_000009.10:g.37426955A>G	NCBI36
NG_008135.1:g.19249A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*176A>G MANE Select	ENSP00000313432.6:n.*176A>G
ENST00000318158.10:c.*176A>G	ENSP00000313432.6:n.*176A>G
ENST00000480596.5:n.1864A>G
ENST00000494290.1:c.*129A>G	ENSP00000432021.1:n.*129A>G
ENST00000497693.1:n.4731A>G
NM_012203.1:c.*176A>G	NP_036335.1:n.*176A>G
XM_005251631.1:c.*176A>G	XP_005251688.1:n.*176A>G
XM_011518073.1:c.*176A>G	XP_011516375.1:n.*176A>G
XM_017015320.2:c.946-453A>G	XP_016870809.1:n.946-453A>G
XM_017015321.2:c.866-453A>G	XP_016870810.1:n.866-453A>G
XM_017015323.2:c.544-453A>G	XP_016870812.1:n.544-453A>G
XM_024447716.1:c.1219-453A>G	XP_024303484.1:n.1219-453A>G
XM_024447717.1:c.1139-453A>G	XP_024303485.1:n.1139-453A>G
XR_002956828.1:n.1234-453A>G
XR_002956829.1:n.1154-453A>G
XR_002956830.1:n.2583A>G
XR_002956831.1:n.2258A>G
XR_002956832.1:n.1582A>G
NM_012203.2:c.*176A>G MANE Select	NP_036335.1:n.*176A>G