Canonical Allele Identifier: CA373442758

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428521T>C (hg19) ; chr9:g.37428524T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428524T>C , CM000671.2:g.37428524T>C	GRCh38
NC_000009.11:g.37428521T>C , CM000671.1:g.37428521T>C	GRCh37
NC_000009.10:g.37418521T>C	NCBI36
NG_008135.1:g.10815T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.445T>C MANE Select	ENSP00000313432.6:p.Tyr149His
ENST00000318158.10:c.445T>C	ENSP00000313432.6:p.Tyr149His
ENST00000377824.8:n.482T>C
ENST00000460882.5:n.472T>C
ENST00000491488.5:n.150T>C
ENST00000493368.5:n.502T>C
ENST00000497693.1:n.819T>C
ENST00000607784.1:c.445T>C	ENSP00000475569.1:p.Tyr149His
NM_012203.1:c.445T>C	NP_036335.1:p.Tyr149His
XM_005251631.1:c.124T>C	XP_005251688.1:p.Tyr42His
XM_011518073.1:c.-318T>C	XP_011516375.1:n.-318T>C
XR_929374.1:n.530T>C
XM_017015320.2:c.445T>C	XP_016870809.1:p.Tyr149His
XM_017015321.2:c.445T>C	XP_016870810.1:p.Tyr149His
XM_017015323.2:c.-318T>C	XP_016870812.1:n.-318T>C
XM_024447716.1:c.718T>C	XP_024303484.1:p.Tyr240His
XM_024447717.1:c.718T>C	XP_024303485.1:p.Tyr240His
XR_002956828.1:n.733T>C
XR_002956829.1:n.733T>C
XR_002956830.1:n.504T>C
XR_002956831.1:n.179T>C
XR_002956832.1:n.504T>C
NM_012203.2:c.445T>C MANE Select	NP_036335.1:p.Tyr149His