Canonical Allele Identifier: CA1846887159
Gene: GRHPR HGNC NCBI

Linked Data

dbSNP Id: rs1219127334
gnomAD v4: 9-37436992-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436992A>T , CM000671.2:g.37436992A>T GRCh38
NC_000009.11:g.37436989A>T , CM000671.1:g.37436989A>T GRCh37
NC_000009.10:g.37426989A>T NCBI36
NG_008135.1:g.19283A>T

Transcript Alleles

HGVS Amino-acid Change
XM_005251631.1:c.*210A>T XP_005251688.1:n.*210A>T
XM_011518073.1:c.*210A>T XP_011516375.1:n.*210A>T
XM_017015320.2:c.946-419A>T XP_016870809.1:n.946-419A>T
XM_017015321.2:c.866-419A>T XP_016870810.1:n.866-419A>T
XM_017015323.2:c.544-419A>T XP_016870812.1:n.544-419A>T
XM_024447716.1:c.1219-419A>T XP_024303484.1:n.1219-419A>T
XM_024447717.1:c.1139-419A>T XP_024303485.1:n.1139-419A>T
XR_002956828.1:n.1234-419A>T
XR_002956829.1:n.1154-419A>T
XR_002956830.1:n.2617A>T
XR_002956831.1:n.2292A>T
XR_002956832.1:n.1616A>T