Canonical Allele Identifier: CA192896355

Gene: GRHPR

Linked Data

• dbSNP Id: rs1030071327
• gnomAD v3: 9-37436968-T-C
• gnomAD v4: 9-37436968-T-C
• MyVariant Identifiers: chr9:g.37436965T>C (hg19) ; chr9:g.37436968T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436968T>C , CM000671.2:g.37436968T>C	GRCh38
NC_000009.11:g.37436965T>C , CM000671.1:g.37436965T>C	GRCh37
NC_000009.10:g.37426965T>C	NCBI36
NG_008135.1:g.19259T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*186T>C MANE Select	ENSP00000313432.6:n.*186T>C
ENST00000318158.10:c.*186T>C	ENSP00000313432.6:n.*186T>C
ENST00000480596.5:n.1874T>C
ENST00000494290.1:c.*139T>C	ENSP00000432021.1:n.*139T>C
ENST00000497693.1:n.4741T>C
NM_012203.1:c.*186T>C	NP_036335.1:n.*186T>C
XM_005251631.1:c.*186T>C	XP_005251688.1:n.*186T>C
XM_011518073.1:c.*186T>C	XP_011516375.1:n.*186T>C
XM_017015320.2:c.946-443T>C	XP_016870809.1:n.946-443T>C
XM_017015321.2:c.866-443T>C	XP_016870810.1:n.866-443T>C
XM_017015323.2:c.544-443T>C	XP_016870812.1:n.544-443T>C
XM_024447716.1:c.1219-443T>C	XP_024303484.1:n.1219-443T>C
XM_024447717.1:c.1139-443T>C	XP_024303485.1:n.1139-443T>C
XR_002956828.1:n.1234-443T>C
XR_002956829.1:n.1154-443T>C
XR_002956830.1:n.2593T>C
XR_002956831.1:n.2268T>C
XR_002956832.1:n.1592T>C
NM_012203.2:c.*186T>C MANE Select	NP_036335.1:n.*186T>C