Linked Data
MyVariant Identifiers:
chr10:g.101611304T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99851547T>C , CM000672.2:g.99851547T>C | GRCh38 |
| NC_000010.10:g.101611304T>C , CM000672.1:g.101611304T>C | GRCh37 |
| NC_000010.9:g.101601294T>C | NCBI36 |
| NG_011798.1:g.73842T>C | |
| NG_011798.2:g.73950T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647814.1:c.4554T>C MANE Select | ENSP00000497274.1:p.Pro1518= | |
| ENST00000648523.1:c.624T>C | ||
| ENST00000370449.8:c.4554T>C | ENSP00000359478.4:p.Pro1518= | |
| NM_000392.4:c.4554T>C | NP_000383.1:p.Pro1518= | |
| XM_006717630.2:c.3858T>C | XP_006717693.1:p.Pro1286= | |
| NM_000392.5:c.4554T>C MANE Select | NP_000383.2:p.Pro1518= | |
| XM_006717630.3:c.3858T>C | XP_006717693.1:p.Pro1286= |