Linked Data
gnomAD v4:
10-99836268-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99836268T>C , CM000672.2:g.99836268T>C | GRCh38 |
| NC_000010.10:g.101596025T>C , CM000672.1:g.101596025T>C | GRCh37 |
| NC_000010.9:g.101586015T>C | NCBI36 |
| NG_011798.1:g.58563T>C | |
| NG_011798.2:g.58671T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3592T>C MANE Select | ENSP00000497274.1:p.Phe1198Leu | |
| ENST00000370449.8:c.3592T>C | ENSP00000359478.4:p.Phe1198Leu | |
| NM_000392.4:c.3592T>C | NP_000383.1:p.Phe1198Leu | |
| XM_006717630.2:c.2896T>C | XP_006717693.1:p.Phe966Leu | |
| XR_945604.1:n.3781T>C | ||
| XR_945605.1:n.3783T>C | ||
| NM_000392.5:c.3592T>C MANE Select | NP_000383.2:p.Phe1198Leu | |
| XM_006717630.3:c.2896T>C | XP_006717693.1:p.Phe966Leu | |
| XR_945604.3:n.3835T>C | ||
| XR_945605.3:n.3835T>C |