Linked Data
dbSNP Id:
rs2041194919
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97611441G>C , CM000672.2:g.97611441G>C | GRCh38 |
| NC_000010.10:g.99371198G>C , CM000672.1:g.99371198G>C | GRCh37 |
| NC_000010.9:g.99361188G>C | NCBI36 |
| NG_027922.1:g.32097G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370646.9:c.835-69G>C MANE Select | ENSP00000359680.4:n.835-69G>C | |
| ENST00000370646.8:c.835-69G>C | ENSP00000359680.4:n.835-69G>C | |
| ENST00000370647.8:c.346-69G>C | ENSP00000359681.4:n.346-69G>C | |
| ENST00000370649.3:c.345+9451G>C | ENSP00000359683.3:n.345+9451G>C | |
| NM_001134670.1:c.346-69G>C | NP_001128142.1:n.346-69G>C | |
| NM_138413.3:c.835-69G>C | NP_612422.2:n.835-69G>C | |
| NM_138413.4:c.835-69G>C MANE Select | NP_612422.2:n.835-69G>C | |
| NM_001134670.2:c.346-69G>C | NP_001128142.1:n.346-69G>C |