Linked Data
gnomAD v4:
X-47574775-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.47574775T>C , CM000685.2:g.47574775T>C | GRCh38 |
| NC_000023.10:g.47434174T>C , CM000685.1:g.47434174T>C | GRCh37 |
| NC_000023.9:g.47319118T>C | NCBI36 |
| NG_008437.1:g.50083A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295987.13:c.1306A>G MANE Select | ENSP00000295987.7:p.Thr436Ala | |
| ENST00000340666.5:c.1306A>G | ENSP00000343206.4:p.Thr436Ala | |
| ENST00000295987.11:c.1306A>G | ENSP00000295987.7:p.Thr436Ala | |
| ENST00000340666.4:c.1306A>G | ENSP00000343206.4:p.Thr436Ala | |
| NM_006950.3:c.1306A>G MANE Select | NP_008881.2:p.Thr436Ala | |
| NM_133499.2:c.1306A>G | NP_598006.1:p.Thr436Ala |