Linked Data
gnomAD v4:
15-68335735-G-T
COSMIC:
COSM6077859
MyVariant Identifiers:
chr15:g.68628073G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68335735G>T , CM000677.2:g.68335735G>T | GRCh38 |
| NC_000015.9:g.68628073G>T , CM000677.1:g.68628073G>T | GRCh37 |
| NC_000015.8:g.66415127G>T | NCBI36 |
| NG_046911.1:g.101426C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000315757.9:c.1387C>A MANE Select | ENSP00000327290.7:p.Arg463= | |
| ENST00000315757.8:c.1387C>A | ENSP00000327290.7:p.Arg463= | |
| ENST00000423218.6:c.1387C>A | ENSP00000403392.2:p.Arg463= | |
| ENST00000566429.1:n.276C>A | ||
| ENST00000569346.5:n.366C>A | ||
| NM_001004439.1:c.1387C>A | NP_001004439.1:p.Arg463= | |
| XM_005254228.2:c.1081C>A | XP_005254285.1:p.Arg361= | |
| XM_011521363.1:c.1180C>A | XP_011519665.1:p.Arg394= | |
| XM_005254228.3:c.1081C>A | XP_005254285.1:p.Arg361= | |
| XM_011521363.2:c.1180C>A | XP_011519665.1:p.Arg394= | |
| NM_001004439.2:c.1387C>A MANE Select | NP_001004439.1:p.Arg463= |