Canonical Allele Identifier: CA188480063

Gene: PLGRKT

Linked Data

• dbSNP Id: rs981980748
• gnomAD v3: 9-5372601-C-T
• gnomAD v4: 9-5372601-C-T
• MyVariant Identifiers: chr9:g.5372601C>T (hg19) ; chr9:g.5372601C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5372601C>T , CM000671.2:g.5372601C>T	GRCh38
NC_000009.11:g.5372601C>T , CM000671.1:g.5372601C>T	GRCh37
NC_000009.10:g.5362601C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223864.7:c.82-10713G>A MANE Select	ENSP00000223864.2:n.82-10713G>A
ENST00000223864.6:c.82-10713G>A	ENSP00000223864.2:n.82-10713G>A
ENST00000472145.5:n.289-10713G>A
ENST00000482696.5:n.461+9262G>A
NM_018465.3:c.82-10713G>A	NP_060935.2:n.82-10713G>A
XM_005251510.3:c.82-10713G>A	XP_005251567.1:n.82-10713G>A
XM_005251512.3:c.-19+9262G>A	XP_005251569.1:n.-19+9262G>A
XM_011517960.1:c.82-10713G>A	XP_011516262.1:n.82-10713G>A
XM_005251510.5:c.82-10713G>A	XP_005251567.1:n.82-10713G>A
XM_005251512.4:c.-19+9262G>A	XP_005251569.1:n.-19+9262G>A
XM_011517960.2:c.82-10713G>A	XP_011516262.1:n.82-10713G>A
NM_018465.4:c.82-10713G>A MANE Select	NP_060935.2:n.82-10713G>A