Canonical Allele Identifier: CA2579340654

Gene: GRHPR

Linked Data

• dbSNP Id: rs2118872500
• gnomAD v4: 9-37428447-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428447G>C , CM000671.2:g.37428447G>C	GRCh38
NC_000009.11:g.37428444G>C , CM000671.1:g.37428444G>C	GRCh37
NC_000009.10:g.37418444G>C	NCBI36
NG_008135.1:g.10738G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-37G>C MANE Select	ENSP00000313432.6:n.405-37G>C
ENST00000318158.10:c.405-37G>C	ENSP00000313432.6:n.405-37G>C
ENST00000377824.8:n.442-37G>C
ENST00000460882.5:n.432-37G>C
ENST00000491488.5:n.110-37G>C
ENST00000493368.5:n.462-37G>C
ENST00000497693.1:n.742G>C
ENST00000607784.1:c.405-37G>C	ENSP00000475569.1:n.405-37G>C
NM_012203.1:c.405-37G>C	NP_036335.1:n.405-37G>C
XM_005251631.1:c.84-37G>C	XP_005251688.1:n.84-37G>C
XM_011518073.1:c.-358-37G>C	XP_011516375.1:n.-358-37G>C
XR_929374.1:n.490-37G>C
XM_017015320.2:c.405-37G>C	XP_016870809.1:n.405-37G>C
XM_017015321.2:c.405-37G>C	XP_016870810.1:n.405-37G>C
XM_017015323.2:c.-358-37G>C	XP_016870812.1:n.-358-37G>C
XM_024447716.1:c.678-37G>C	XP_024303484.1:n.678-37G>C
XM_024447717.1:c.678-37G>C	XP_024303485.1:n.678-37G>C
XR_002956828.1:n.693-37G>C
XR_002956829.1:n.693-37G>C
XR_002956830.1:n.464-37G>C
XR_002956831.1:n.139-37G>C
XR_002956832.1:n.464-37G>C
NM_012203.2:c.405-37G>C MANE Select	NP_036335.1:n.405-37G>C