Linked Data
MyVariant Identifiers:
chr16:g.81399072T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81365467T>C , CM000678.2:g.81365467T>C | GRCh38 |
| NC_000016.9:g.81399072T>C , CM000678.1:g.81399072T>C | GRCh37 |
| NC_000016.8:g.79956573T>C | NCBI36 |
| NG_009007.1:g.55502T>C , LRG_242:g.55502T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*1199T>C | ENSP00000498114.1:n.*1199T>C | |
| ENST00000648994.2:c.1491T>C MANE Select | ENSP00000497351.1:p.Asp497= | |
| ENST00000650388.1:c.1025T>C | ENSP00000498081.1:n.1025T>C | |
| ENST00000567335.1:n.49T>C | ||
| ENST00000568107.2:c.1491T>C | ENSP00000476795.1:p.Asp497= | |
| NM_022041.3:c.1491T>C , LRG_242t1:c.1491T>C | NP_071324.1:p.Asp497= | |
| XM_017023734.1:c.852T>C | XP_016879223.1:p.Asp284= | |
| NM_001377486.1:c.852T>C | NP_001364415.1:p.Asp284= | |
| NM_022041.4:c.1491T>C MANE Select | NP_071324.1:p.Asp497= |