Canonical Allele Identifier: CA188512498
Gene: PLGRKT HGNC NCBI

Linked Data

dbSNP Id: rs1535454
gnomAD v2: 9-5410723-C-T
gnomAD v3: 9-5410723-C-T
gnomAD v4: 9-5410723-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5410723C>T , CM000671.2:g.5410723C>T GRCh38
NC_000009.11:g.5410723C>T , CM000671.1:g.5410723C>T GRCh37
NC_000009.10:g.5400723C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000223864.7:c.81+21174G>A MANE Select ENSP00000223864.2:n.81+21174G>A
ENST00000223864.6:c.81+21174G>A ENSP00000223864.2:n.81+21174G>A
ENST00000472145.5:n.288+21174G>A
ENST00000473877.1:n.214-18074G>A
ENST00000482696.5:n.292+21174G>A
NM_018465.3:c.81+21174G>A NP_060935.2:n.81+21174G>A
XM_005251510.3:c.81+21174G>A XP_005251567.1:n.81+21174G>A
XM_011517960.1:c.81+21174G>A XP_011516262.1:n.81+21174G>A
XM_005251510.5:c.81+21174G>A XP_005251567.1:n.81+21174G>A
XM_011517960.2:c.81+21174G>A XP_011516262.1:n.81+21174G>A
NM_018465.4:c.81+21174G>A MANE Select NP_060935.2:n.81+21174G>A