Canonical Allele Identifier: CA863723564

Gene: GRHPR

Linked Data

• dbSNP Id: rs1441974938
• gnomAD v3: 9-37436986-TGA-T
• gnomAD v4: 9-37436986-TGA-T
• MyVariant Identifiers: chr9:g.37436984_37436985del (hg19) ; chr9:g.37436987_37436988del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436991_37436992del , CM000671.2:g.37436991_37436992del	GRCh38
NC_000009.11:g.37436988_37436989del , CM000671.1:g.37436988_37436989del	GRCh37
NC_000009.10:g.37426988_37426989del	NCBI36
NG_008135.1:g.19282_19283del

Transcript Alleles

HGVS	Amino-acid Change
XM_005251631.1:c.*209_*210del	XP_005251688.1:n.*209_*210del
XM_011518073.1:c.*209_*210del	XP_011516375.1:n.*209_*210del
XM_017015320.2:c.946-420_946-419del	XP_016870809.1:n.946-420_946-419del
XM_017015321.2:c.866-420_866-419del	XP_016870810.1:n.866-420_866-419del
XM_017015323.2:c.544-420_544-419del	XP_016870812.1:n.544-420_544-419del
XM_024447716.1:c.1219-420_1219-419del	XP_024303484.1:n.1219-420_1219-419del
XM_024447717.1:c.1139-420_1139-419del	XP_024303485.1:n.1139-420_1139-419del
XR_002956828.1:n.1234-420_1234-419del
XR_002956829.1:n.1154-420_1154-419del
XR_002956830.1:n.2616_2617del
XR_002956831.1:n.2291_2292del
XR_002956832.1:n.1615_1616del