Canonical Allele Identifier: CA373442137

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37425941-C-G
• MyVariant Identifiers: chr9:g.37425938C>G (hg19) ; chr9:g.37425941C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425941C>G , CM000671.2:g.37425941C>G	GRCh38
NC_000009.11:g.37425938C>G , CM000671.1:g.37425938C>G	GRCh37
NC_000009.10:g.37415938C>G	NCBI36
NG_008135.1:g.8232C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.234C>G MANE Select	ENSP00000313432.6:p.Ile78Met
ENST00000318158.10:c.234C>G	ENSP00000313432.6:p.Ile78Met
ENST00000377824.8:n.271C>G
ENST00000460882.5:n.261C>G
ENST00000487399.5:n.243C>G
ENST00000491488.5:n.110-2543C>G
ENST00000493368.5:n.291C>G
ENST00000607784.1:c.234C>G	ENSP00000475569.1:p.Ile78Met
NM_012203.1:c.234C>G	NP_036335.1:p.Ile78Met
XM_005251631.1:c.84-2543C>G	XP_005251688.1:n.84-2543C>G
XM_011518073.1:c.-529C>G	XP_011516375.1:n.-529C>G
XR_929374.1:n.319C>G
XM_017015320.2:c.234C>G	XP_016870809.1:p.Ile78Met
XM_017015321.2:c.234C>G	XP_016870810.1:p.Ile78Met
XM_017015323.2:c.-529C>G	XP_016870812.1:n.-529C>G
XM_024447716.1:c.507C>G	XP_024303484.1:p.Ile169Met
XM_024447717.1:c.507C>G	XP_024303485.1:p.Ile169Met
XR_002956828.1:n.522C>G
XR_002956829.1:n.522C>G
XR_002956830.1:n.293C>G
XR_002956831.1:n.139-2543C>G
XR_002956832.1:n.293C>G
NM_012203.2:c.234C>G MANE Select	NP_036335.1:p.Ile78Met