Canonical Allele Identifier: CA5059243
Gene: GRHPR HGNC NCBI

Linked Data

dbSNP Id: rs368088674
gnomAD v2: 9-37431967-G-A
gnomAD v3: 9-37431970-G-A
gnomAD v4: 9-37431970-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37431970G>A , CM000671.2:g.37431970G>A GRCh38
NC_000009.11:g.37431967G>A , CM000671.1:g.37431967G>A GRCh37
NC_000009.10:g.37421967G>A NCBI36
NG_008135.1:g.14261G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.735-38G>A MANE Select ENSP00000313432.6:n.735-38G>A
ENST00000318158.10:c.735-38G>A ENSP00000313432.6:n.735-38G>A
ENST00000460882.5:n.762-38G>A
ENST00000480596.5:n.1436-38G>A
ENST00000482603.1:n.188-38G>A
ENST00000491488.5:n.440-38G>A
ENST00000494290.1:c.*51+819G>A ENSP00000432021.1:n.*51+819G>A
ENST00000497693.1:n.4265G>A
ENST00000607784.1:c.735-38G>A ENSP00000475569.1:n.735-38G>A
NM_012203.1:c.735-38G>A NP_036335.1:n.735-38G>A
XM_005251631.1:c.414-38G>A XP_005251688.1:n.414-38G>A
XM_011518073.1:c.333-38G>A XP_011516375.1:n.333-38G>A
XM_017015320.2:c.735-38G>A XP_016870809.1:n.735-38G>A
XM_017015321.2:c.735-38G>A XP_016870810.1:n.735-38G>A
XM_017015323.2:c.333-38G>A XP_016870812.1:n.333-38G>A
XM_024447716.1:c.1008-38G>A XP_024303484.1:n.1008-38G>A
XM_024447717.1:c.1008-38G>A XP_024303485.1:n.1008-38G>A
XR_002956828.1:n.1023-38G>A
XR_002956829.1:n.1023-38G>A
XR_002956830.1:n.2117G>A
XR_002956831.1:n.1792G>A
XR_002956832.1:n.1154-38G>A
NM_012203.2:c.735-38G>A MANE Select NP_036335.1:n.735-38G>A