Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102838694A>G , CM000673.2:g.102838694A>G | GRCh38 |
| NC_000011.9:g.102709425A>G , CM000673.1:g.102709425A>G | GRCh37 |
| NC_000011.8:g.102214635A>G | NCBI36 |
| NG_012100.1:g.9918T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299855.10:c.1086T>C MANE Select | ENSP00000299855.5:p.Ala362= | |
| ENST00000299855.9:c.1086T>C | ENSP00000299855.5:p.Ala362= | |
| ENST00000434103.1:c.17T>C | ||
| NM_002422.3:c.1086T>C | NP_002413.1:p.Ala362= | |
| NM_002422.4:c.1086T>C | NP_002413.1:p.Ala362= | |
| NM_002422.5:c.1086T>C MANE Select | NP_002413.1:p.Ala362= |