Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99844392A>C , CM000672.2:g.99844392A>C | GRCh38 |
| NC_000010.10:g.101604149A>C , CM000672.1:g.101604149A>C | GRCh37 |
| NC_000010.9:g.101594139A>C | NCBI36 |
| NG_011798.1:g.66687A>C | |
| NG_011798.2:g.66795A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3914A>C MANE Select | ENSP00000497274.1:p.Tyr1305Ser | |
| ENST00000649459.1:n.262A>C | ||
| ENST00000370449.8:c.3914A>C | ENSP00000359478.4:p.Tyr1305Ser | |
| NM_000392.4:c.3914A>C | NP_000383.1:p.Tyr1305Ser | |
| XM_006717630.2:c.3218A>C | XP_006717693.1:p.Tyr1073Ser | |
| XR_945604.1:n.4103A>C | ||
| XR_945605.1:n.3978A>C | ||
| NM_000392.5:c.3914A>C MANE Select | NP_000383.2:p.Tyr1305Ser | |
| XM_006717630.3:c.3218A>C | XP_006717693.1:p.Tyr1073Ser | |
| XR_945604.3:n.4157A>C | ||
| XR_945605.3:n.4030A>C |