Linked Data
gnomAD v4:
12-101761704-C-T
COSMIC:
COSM1358183
MyVariant Identifiers:
chr12:g.102155482C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101761704C>T , CM000674.2:g.101761704C>T | GRCh38 |
| NC_000012.11:g.102155482C>T , CM000674.1:g.102155482C>T | GRCh37 |
| NC_000012.10:g.100679613C>T | NCBI36 |
| NG_021243.1:g.74164G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.2775G>A MANE Select | ENSP00000299314.7:p.Arg925= | |
| ENST00000299314.11:c.2775G>A | ENSP00000299314.7:p.Arg925= | |
| NM_024312.4:c.2775G>A | NP_077288.2:p.Arg925= | |
| XM_006719593.2:c.2775G>A | XP_006719656.1:p.Arg925= | |
| XM_011538731.1:c.2694G>A | XP_011537033.1:p.Arg898= | |
| XM_006719593.3:c.2775G>A | XP_006719656.1:p.Arg925= | |
| XM_011538731.2:c.2694G>A | XP_011537033.1:p.Arg898= | |
| XM_017019961.1:c.2559G>A | XP_016875450.1:p.Arg853= | |
| XM_017019962.2:c.1548G>A | XP_016875451.1:p.Arg516= | |
| NM_024312.5:c.2775G>A MANE Select | NP_077288.2:p.Arg925= |