Linked Data
gnomAD v4:
10-99836275-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99836275G>C , CM000672.2:g.99836275G>C | GRCh38 |
| NC_000010.10:g.101596032G>C , CM000672.1:g.101596032G>C | GRCh37 |
| NC_000010.9:g.101586022G>C | NCBI36 |
| NG_011798.1:g.58570G>C | |
| NG_011798.2:g.58678G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3599G>C MANE Select | ENSP00000497274.1:p.Trp1200Ser | |
| ENST00000370449.8:c.3599G>C | ENSP00000359478.4:p.Trp1200Ser | |
| NM_000392.4:c.3599G>C | NP_000383.1:p.Trp1200Ser | |
| XM_006717630.2:c.2903G>C | XP_006717693.1:p.Trp968Ser | |
| XR_945604.1:n.3788G>C | ||
| XR_945605.1:n.3790G>C | ||
| NM_000392.5:c.3599G>C MANE Select | NP_000383.2:p.Trp1200Ser | |
| XM_006717630.3:c.2903G>C | XP_006717693.1:p.Trp968Ser | |
| XR_945604.3:n.3842G>C | ||
| XR_945605.3:n.3842G>C |