Canonical Allele Identifier: CA863720634

Gene: GRHPR

Linked Data

• dbSNP Id: rs775584090
• MyVariant Identifiers: chr9:g.37432147A>C (hg19) ; chr9:g.37432150A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432150A>C , CM000671.2:g.37432150A>C	GRCh38
NC_000009.11:g.37432147A>C , CM000671.1:g.37432147A>C	GRCh37
NC_000009.10:g.37422147A>C	NCBI36
NG_008135.1:g.14441A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.865+12A>C MANE Select	ENSP00000313432.6:n.865+12A>C
ENST00000318158.10:c.865+12A>C	ENSP00000313432.6:n.865+12A>C
ENST00000460882.5:n.892+12A>C
ENST00000480596.5:n.1566+12A>C
ENST00000482603.1:n.318+12A>C
ENST00000491488.5:n.570+12A>C
ENST00000494290.1:c.*51+999A>C	ENSP00000432021.1:n.*51+999A>C
ENST00000497693.1:n.4433+12A>C
ENST00000512404.2:n.64A>C
ENST00000607784.1:c.865+12A>C	ENSP00000475569.1:n.865+12A>C
NM_012203.1:c.865+12A>C	NP_036335.1:n.865+12A>C
XM_005251631.1:c.544+12A>C	XP_005251688.1:n.544+12A>C
XM_011518073.1:c.463+12A>C	XP_011516375.1:n.463+12A>C
XM_017015320.2:c.865+12A>C	XP_016870809.1:n.865+12A>C
XM_017015321.2:c.865+12A>C	XP_016870810.1:n.865+12A>C
XM_017015323.2:c.463+12A>C	XP_016870812.1:n.463+12A>C
XM_024447716.1:c.1138+12A>C	XP_024303484.1:n.1138+12A>C
XM_024447717.1:c.1138+12A>C	XP_024303485.1:n.1138+12A>C
XR_002956828.1:n.1153+12A>C
XR_002956829.1:n.1153+12A>C
XR_002956830.1:n.2285+12A>C
XR_002956831.1:n.1960+12A>C
XR_002956832.1:n.1284+12A>C
NM_012203.2:c.865+12A>C MANE Select	NP_036335.1:n.865+12A>C