Canonical Allele Identifier: CA465006836

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436710C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436713C>T , CM000671.2:g.37436713C>T	GRCh38
NC_000009.11:g.37436710C>T , CM000671.1:g.37436710C>T	GRCh37
NC_000009.10:g.37426710C>T	NCBI36
NG_008135.1:g.19004C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.918C>T MANE Select	ENSP00000313432.6:p.Ser306=
ENST00000318158.10:c.918C>T	ENSP00000313432.6:p.Ser306=
ENST00000460882.5:n.945C>T
ENST00000480596.5:n.1619C>T
ENST00000494290.1:c.*52-168C>T	ENSP00000432021.1:n.*52-168C>T
ENST00000497693.1:n.4486C>T
NM_012203.1:c.918C>T	NP_036335.1:p.Ser306=
XM_005251631.1:c.597C>T	XP_005251688.1:p.Ser199=
XM_011518073.1:c.516C>T	XP_011516375.1:p.Ser172=
XM_017015320.2:c.946-698C>T	XP_016870809.1:n.946-698C>T
XM_017015321.2:c.866-698C>T	XP_016870810.1:n.866-698C>T
XM_017015323.2:c.544-698C>T	XP_016870812.1:n.544-698C>T
XM_024447716.1:c.1219-698C>T	XP_024303484.1:n.1219-698C>T
XM_024447717.1:c.1139-698C>T	XP_024303485.1:n.1139-698C>T
XR_002956828.1:n.1234-698C>T
XR_002956829.1:n.1154-698C>T
XR_002956830.1:n.2338C>T
XR_002956831.1:n.2013C>T
XR_002956832.1:n.1337C>T
NM_012203.2:c.918C>T MANE Select	NP_036335.1:p.Ser306=