Canonical Allele Identifier: CA188479894
Gene: PLGRKT HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17501809

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5372411G>A , CM000671.2:g.5372411G>A GRCh38
NC_000009.10:g.5362411G>A NCBI36
NC_000009.11:g.5372411G>A , CM000671.1:g.5372411G>A GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000223864.6:c.82-10523C>T ENSP00000223864.2:p.=
ENST00000472145.5:n.289-10523C>T
ENST00000482696.5:n.461+9452C>T
NM_018465.3:c.82-10523C>T VV NP_060935.2:p.=
XM_005251510.3:c.82-10523C>T XP_005251567.1:p.=
XM_005251512.3:c.-19+9452C>T XP_005251569.1:p.=
XM_011517960.1:c.82-10523C>T XP_011516262.1:p.=
XM_005251510.5:c.82-10523C>T
XM_005251512.4:c.-19+9452C>T
XM_011517960.2:c.82-10523C>T