Linked Data
gnomAD v4:
7-17339804-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17339804T>C , CM000669.2:g.17339804T>C | GRCh38 |
| NC_000007.13:g.17379428T>C , CM000669.1:g.17379428T>C | GRCh37 |
| NC_000007.12:g.17345953T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242057.9:c.1979T>C MANE Select | ENSP00000242057.4:p.Val660Ala | |
| ENST00000637807.1:c.1949T>C | ENSP00000490530.1:p.Val650Ala | |
| ENST00000642825.1:c.1934T>C | ENSP00000495987.1:p.Val645Ala | |
| ENST00000242057.8:c.1979T>C | ENSP00000242057.4:p.Val660Ala | |
| ENST00000463496.1:c.1979T>C | ENSP00000436466.1:p.Val660Ala | |
| NM_001621.4:c.1979T>C | NP_001612.1:p.Val660Ala | |
| NM_001621.5:c.1979T>C MANE Select | NP_001612.1:p.Val660Ala |