Canonical Allele Identifier: CA2719474833

Gene: GRHPR

Linked Data

• dbSNP Id: rs2118917454

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436857A>C , CM000671.2:g.37436857A>C	GRCh38
NC_000009.11:g.37436854A>C , CM000671.1:g.37436854A>C	GRCh37
NC_000009.10:g.37426854A>C	NCBI36
NG_008135.1:g.19148A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*75A>C MANE Select	ENSP00000313432.6:n.*75A>C
ENST00000318158.10:c.*75A>C	ENSP00000313432.6:n.*75A>C
ENST00000480596.5:n.1763A>C
ENST00000494290.1:c.*52-24A>C	ENSP00000432021.1:n.*52-24A>C
ENST00000497693.1:n.4630A>C
NM_012203.1:c.*75A>C	NP_036335.1:n.*75A>C
XM_005251631.1:c.*75A>C	XP_005251688.1:n.*75A>C
XM_011518073.1:c.*75A>C	XP_011516375.1:n.*75A>C
XM_017015320.2:c.946-554A>C	XP_016870809.1:n.946-554A>C
XM_017015321.2:c.866-554A>C	XP_016870810.1:n.866-554A>C
XM_017015323.2:c.544-554A>C	XP_016870812.1:n.544-554A>C
XM_024447716.1:c.1219-554A>C	XP_024303484.1:n.1219-554A>C
XM_024447717.1:c.1139-554A>C	XP_024303485.1:n.1139-554A>C
XR_002956828.1:n.1234-554A>C
XR_002956829.1:n.1154-554A>C
XR_002956830.1:n.2482A>C
XR_002956831.1:n.2157A>C
XR_002956832.1:n.1481A>C
NM_012203.2:c.*75A>C MANE Select	NP_036335.1:n.*75A>C