Linked Data
dbSNP Id:
rs1569560005
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154996943G>A , CM000685.2:g.154996943G>A | GRCh38 |
| NC_000023.10:g.154225218G>A , CM000685.1:g.154225218G>A | GRCh37 |
| NC_000023.9:g.153878412G>A | NCBI36 |
| NG_011403.1:g.30781C>T | |
| NG_011403.2:g.30781C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.388+30C>T MANE Select | ENSP00000353393.4:n.388+30C>T | |
| ENST00000647125.1:c.*174+30C>T | ENSP00000496062.1:n.*174+30C>T | |
| ENST00000360256.8:c.388+30C>T | ENSP00000353393.4:n.388+30C>T | |
| ENST00000423959.5:c.283+30C>T | ENSP00000409446.1:n.283+30C>T | |
| ENST00000453950.1:c.370+30C>T | ENSP00000389153.1:n.370+30C>T | |
| NM_000132.3:c.388+30C>T | NP_000123.1:n.388+30C>T | |
| XM_011531126.1:c.283+30C>T | XP_011529428.1:n.283+30C>T | |
| NM_000132.4:c.388+30C>T MANE Select | NP_000123.1:n.388+30C>T |