Linked Data
dbSNP Id:
rs866819648
gnomAD v2:
10-120970155-T-C
gnomAD v3:
10-119210643-T-C
gnomAD v4:
10-119210643-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119210643T>C , CM000672.2:g.119210643T>C | GRCh38 |
| NC_000010.10:g.120970155T>C , CM000672.1:g.120970155T>C | GRCh37 |
| NC_000010.9:g.120960145T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392870.3:c.52+2674T>C (GRK5) MANE Select | ENSP00000376609.2:n.52+2674T>C | |
| ENST00000392870.2:c.52+2674T>C (GRK5) | ENSP00000376609.2:n.52+2674T>C | |
| NM_005308.2:c.52+2674T>C (GRK5) | NP_005299.1:n.52+2674T>C | |
| XM_005269707.1:c.52+2674T>C (GRK5) | XP_005269764.1:n.52+2674T>C | |
| XM_005269708.1:c.52+2674T>C (GRK5) | XP_005269765.1:n.52+2674T>C | |
| XR_246196.2:n.583-838T>C (GRK5-IT1) | ||
| XM_005269707.2:c.52+2674T>C (GRK5) | XP_005269764.1:n.52+2674T>C | |
| XR_246196.4:n.669-838T>C (GRK5-IT1) | ||
| NM_005308.3:c.52+2674T>C (GRK5) MANE Select | NP_005299.1:n.52+2674T>C |