Canonical Allele Identifier: CA465003854

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37426547T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426550T>G , CM000671.2:g.37426550T>G	GRCh38
NC_000009.11:g.37426547T>G , CM000671.1:g.37426547T>G	GRCh37
NC_000009.10:g.37416547T>G	NCBI36
NG_008135.1:g.8841T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.300T>G MANE Select	ENSP00000313432.6:p.Val100=
ENST00000318158.10:c.300T>G	ENSP00000313432.6:p.Val100=
ENST00000377824.8:n.337T>G
ENST00000460882.5:n.327T>G
ENST00000487399.5:n.852T>G
ENST00000491488.5:n.110-1934T>G
ENST00000493368.5:n.357T>G
ENST00000607784.1:c.300T>G	ENSP00000475569.1:p.Val100=
NM_012203.1:c.300T>G	NP_036335.1:p.Val100=
XM_005251631.1:c.84-1934T>G	XP_005251688.1:n.84-1934T>G
XM_011518073.1:c.-463T>G	XP_011516375.1:n.-463T>G
XR_929374.1:n.385T>G
XM_017015320.2:c.300T>G	XP_016870809.1:p.Val100=
XM_017015321.2:c.300T>G	XP_016870810.1:p.Val100=
XM_017015323.2:c.-463T>G	XP_016870812.1:n.-463T>G
XM_024447716.1:c.573T>G	XP_024303484.1:p.Val191=
XM_024447717.1:c.573T>G	XP_024303485.1:p.Val191=
XR_002956828.1:n.588T>G
XR_002956829.1:n.588T>G
XR_002956830.1:n.359T>G
XR_002956831.1:n.139-1934T>G
XR_002956832.1:n.359T>G
NM_012203.2:c.300T>G MANE Select	NP_036335.1:p.Val100=