Canonical Allele Identifier: CA373445283

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436657G>C (hg19) ; chr9:g.37436660G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436660G>C , CM000671.2:g.37436660G>C	GRCh38
NC_000009.11:g.37436657G>C , CM000671.1:g.37436657G>C	GRCh37
NC_000009.10:g.37426657G>C	NCBI36
NG_008135.1:g.18951G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-1G>C MANE Select	ENSP00000313432.6:n.866-1G>C
ENST00000318158.10:c.866-1G>C	ENSP00000313432.6:n.866-1G>C
ENST00000460882.5:n.893-1G>C
ENST00000480596.5:n.1567-1G>C
ENST00000491488.5:n.571-1G>C
ENST00000494290.1:c.*52-221G>C	ENSP00000432021.1:n.*52-221G>C
ENST00000497693.1:n.4434-1G>C
NM_012203.1:c.866-1G>C	NP_036335.1:n.866-1G>C
XM_005251631.1:c.545-1G>C	XP_005251688.1:n.545-1G>C
XM_011518073.1:c.464-1G>C	XP_011516375.1:n.464-1G>C
XM_017015320.2:c.946-751G>C	XP_016870809.1:n.946-751G>C
XM_017015321.2:c.866-751G>C	XP_016870810.1:n.866-751G>C
XM_017015323.2:c.544-751G>C	XP_016870812.1:n.544-751G>C
XM_024447716.1:c.1219-751G>C	XP_024303484.1:n.1219-751G>C
XM_024447717.1:c.1139-751G>C	XP_024303485.1:n.1139-751G>C
XR_002956828.1:n.1234-751G>C
XR_002956829.1:n.1154-751G>C
XR_002956830.1:n.2286-1G>C
XR_002956831.1:n.1961-1G>C
XR_002956832.1:n.1285-1G>C
NM_012203.2:c.866-1G>C MANE Select	NP_036335.1:n.866-1G>C