Linked Data
MyVariant Identifiers:
chr13:g.20763460T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189321T>C , CM000675.2:g.20189321T>C | GRCh38 |
| NC_000013.10:g.20763460T>C , CM000675.1:g.20763460T>C | GRCh37 |
| NC_000013.9:g.19661460T>C | NCBI36 |
| NG_008358.1:g.8655A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.261A>G | ENSP00000372295.1:p.Pro87= | |
| ENST00000382848.5:c.261A>G MANE Select | ENSP00000372299.4:p.Pro87= | |
| ENST00000382844.1:c.261A>G | ENSP00000372295.1:p.Pro87= | |
| ENST00000382848.4:c.261A>G | ENSP00000372299.4:p.Pro87= | |
| NM_004004.5:c.261A>G | NP_003995.2:p.Pro87= | |
| XM_011535049.1:c.261A>G | XP_011533351.1:p.Pro87= | |
| XM_011535049.2:c.261A>G | XP_011533351.1:p.Pro87= | |
| NM_004004.6:c.261A>G MANE Select | NP_003995.2:p.Pro87= |