Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34256252A>C , CM000679.2:g.34256252A>C | GRCh38 |
| NC_000017.10:g.32583271A>C , CM000679.1:g.32583271A>C | GRCh37 |
| NC_000017.9:g.29607384A>C | NCBI36 |
| NG_012123.1:g.5976A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000580907.6:c.107A>C | ENSP00000462156.1:p.Tyr36Ser | |
| ENST00000624362.2:n.968A>C | ||
| ENST00000225831.4:c.107A>C MANE Select | ENSP00000225831.4:p.Tyr36Ser | |
| ENST00000580907.5:c.107A>C | ENSP00000462156.1:p.Tyr36Ser | |
| ENST00000582017.1:n.45A>C | ||
| NM_002982.3:c.107A>C | NP_002973.1:p.Tyr36Ser | |
| NM_002982.4:c.107A>C MANE Select | NP_002973.1:p.Tyr36Ser |