Canonical Allele Identifier: CA2689984569

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436631-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436631T>C , CM000671.2:g.37436631T>C	GRCh38
NC_000009.11:g.37436628T>C , CM000671.1:g.37436628T>C	GRCh37
NC_000009.10:g.37426628T>C	NCBI36
NG_008135.1:g.18922T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-30T>C MANE Select	ENSP00000313432.6:n.866-30T>C
ENST00000318158.10:c.866-30T>C	ENSP00000313432.6:n.866-30T>C
ENST00000460882.5:n.893-30T>C
ENST00000480596.5:n.1567-30T>C
ENST00000491488.5:n.571-30T>C
ENST00000494290.1:c.*52-250T>C	ENSP00000432021.1:n.*52-250T>C
ENST00000497693.1:n.4434-30T>C
NM_012203.1:c.866-30T>C	NP_036335.1:n.866-30T>C
XM_005251631.1:c.545-30T>C	XP_005251688.1:n.545-30T>C
XM_011518073.1:c.464-30T>C	XP_011516375.1:n.464-30T>C
XM_017015320.2:c.946-780T>C	XP_016870809.1:n.946-780T>C
XM_017015321.2:c.866-780T>C	XP_016870810.1:n.866-780T>C
XM_017015323.2:c.544-780T>C	XP_016870812.1:n.544-780T>C
XM_024447716.1:c.1219-780T>C	XP_024303484.1:n.1219-780T>C
XM_024447717.1:c.1139-780T>C	XP_024303485.1:n.1139-780T>C
XR_002956828.1:n.1234-780T>C
XR_002956829.1:n.1154-780T>C
XR_002956830.1:n.2286-30T>C
XR_002956831.1:n.1961-30T>C
XR_002956832.1:n.1285-30T>C
NM_012203.2:c.866-30T>C MANE Select	NP_036335.1:n.866-30T>C