Linked Data
dbSNP Id:
rs2058300784
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942983G>A , CM000678.2:g.67942983G>A | GRCh38 |
| NC_000016.9:g.67976886G>A , CM000678.1:g.67976886G>A | GRCh37 |
| NC_000016.8:g.66534387G>A | NCBI36 |
| NG_009778.1:g.6130C>T | |
| NG_033098.1:g.30712C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264005.10:c.312-7C>T MANE Select | ENSP00000264005.5:n.312-7C>T | |
| ENST00000264005.9:c.312-7C>T | ENSP00000264005.5:n.312-7C>T | |
| ENST00000570369.5:c.40-7C>T | ||
| ENST00000570980.1:c.96-7C>T | ENSP00000464651.1:n.96-7C>T | |
| ENST00000575277.1:n.90-7C>T | ||
| ENST00000575467.5:c.*7-7C>T | ENSP00000460653.1:n.*7-7C>T | |
| NM_000229.1:c.312-7C>T | NP_000220.1:n.312-7C>T | |
| NM_000229.2:c.312-7C>T MANE Select | NP_000220.1:n.312-7C>T |