Linked Data
dbSNP Id:
rs1961080199
COSMIC:
COSM6464466
MyVariant Identifiers:
chr16:g.68853312C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68819409C>A , CM000678.2:g.68819409C>A | GRCh38 |
| NC_000016.9:g.68853312C>A , CM000678.1:g.68853312C>A | GRCh37 |
| NC_000016.8:g.67410813C>A | NCBI36 |
| NG_008021.1:g.87118C>A , LRG_301:g.87118C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261769.10:c.1695C>A MANE Select | ENSP00000261769.4:p.Ile565= | |
| ENST00000261769.9:c.1695C>A | ENSP00000261769.4:p.Ile565= | |
| ENST00000422392.6:c.1512C>A | ENSP00000414946.2:p.Ile504= | |
| ENST00000562836.5:n.1766C>A | ||
| ENST00000566510.5:c.*361C>A | ENSP00000458139.1:n.*361C>A | |
| ENST00000566612.5:c.1566-2592C>A | ENSP00000454782.1:n.1566-2592C>A | |
| ENST00000611625.4:c.1758C>A | ENSP00000481063.1:p.Ile586= | |
| ENST00000612417.4:c.1695C>A | ENSP00000478360.1:p.Ile565= | |
| ENST00000621016.4:c.1695C>A | ENSP00000480664.1:p.Ile565= | |
| NM_004360.3:c.1695C>A , LRG_301t1:c.1695C>A | NP_004351.1:p.Ile565= | |
| XM_011523488.1:c.960C>A | XP_011521790.1:p.Ile320= | |
| XM_011523489.1:c.960C>A | XP_011521791.1:p.Ile320= | |
| NM_001317184.1:c.1512C>A | NP_001304113.1:p.Ile504= | |
| NM_001317185.1:c.147C>A | NP_001304114.1:p.Ile49= | |
| NM_001317186.1:c.-254-2592C>A | NP_001304115.1:n.-254-2592C>A | |
| NM_004360.4:c.1695C>A | NP_004351.1:p.Ile565= | |
| NM_004360.5:c.1695C>A MANE Select | NP_004351.1:p.Ile565= | |
| NM_001317184.2:c.1512C>A | NP_001304113.1:p.Ile504= | |
| NM_001317185.2:c.147C>A | NP_001304114.1:p.Ile49= | |
| NM_001317186.2:c.-254-2592C>A | NP_001304115.1:n.-254-2592C>A |