Canonical Allele Identifier: CA2689952723

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37425071-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425071G>T , CM000671.2:g.37425071G>T	GRCh38
NC_000009.11:g.37425068G>T , CM000671.1:g.37425068G>T	GRCh37
NC_000009.10:g.37415068G>T	NCBI36
NG_008135.1:g.7362G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.214+96G>T MANE Select	ENSP00000313432.6:n.214+96G>T
ENST00000318158.10:c.214+96G>T	ENSP00000313432.6:n.214+96G>T
ENST00000377824.8:n.251+96G>T
ENST00000460882.5:n.241+96G>T
ENST00000487399.5:n.223+96G>T
ENST00000491488.5:n.109+2238G>T
ENST00000493368.5:n.271+96G>T
ENST00000607784.1:c.214+96G>T	ENSP00000475569.1:n.214+96G>T
NM_012203.1:c.214+96G>T	NP_036335.1:n.214+96G>T
XM_005251631.1:c.83+2238G>T	XP_005251688.1:n.83+2238G>T
XM_011518073.1:c.-549+96G>T	XP_011516375.1:n.-549+96G>T
XR_929374.1:n.299+96G>T
XM_017015320.2:c.214+96G>T	XP_016870809.1:n.214+96G>T
XM_017015321.2:c.214+96G>T	XP_016870810.1:n.214+96G>T
XM_017015323.2:c.-549+96G>T	XP_016870812.1:n.-549+96G>T
XM_024447716.1:c.487+96G>T	XP_024303484.1:n.487+96G>T
XM_024447717.1:c.487+96G>T	XP_024303485.1:n.487+96G>T
XR_002956828.1:n.502+96G>T
XR_002956829.1:n.502+96G>T
XR_002956830.1:n.273+96G>T
XR_002956831.1:n.138+2238G>T
XR_002956832.1:n.273+96G>T
NM_012203.2:c.214+96G>T MANE Select	NP_036335.1:n.214+96G>T