Linked Data
gnomAD v4:
X-25013451-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25013451A>C , CM000685.2:g.25013451A>C | GRCh38 |
| NC_000023.10:g.25031568A>C , CM000685.1:g.25031568A>C | GRCh37 |
| NC_000023.9:g.24941489A>C | NCBI36 |
| NG_008281.1:g.7498T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379044.5:c.544T>G MANE Select | ENSP00000368332.4:p.Phe182Val | |
| ENST00000379044.4:c.544T>G | ENSP00000368332.4:p.Phe182Val | |
| NM_139058.2:c.544T>G | NP_620689.1:p.Phe182Val | |
| NM_139058.3:c.544T>G MANE Select | NP_620689.1:p.Phe182Val |