Linked Data
gnomAD v4:
10-99844427-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99844427C>T , CM000672.2:g.99844427C>T | GRCh38 |
| NC_000010.10:g.101604184C>T , CM000672.1:g.101604184C>T | GRCh37 |
| NC_000010.9:g.101594174C>T | NCBI36 |
| NG_011798.1:g.66722C>T | |
| NG_011798.2:g.66830C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3949C>T MANE Select | ENSP00000497274.1:p.Leu1317Phe | |
| ENST00000649459.1:n.297C>T | ||
| ENST00000370449.8:c.3949C>T | ENSP00000359478.4:p.Leu1317Phe | |
| NM_000392.4:c.3949C>T | NP_000383.1:p.Leu1317Phe | |
| XM_006717630.2:c.3253C>T | XP_006717693.1:p.Leu1085Phe | |
| XR_945604.1:n.4138C>T | ||
| XR_945605.1:n.4013C>T | ||
| NM_000392.5:c.3949C>T MANE Select | NP_000383.2:p.Leu1317Phe | |
| XM_006717630.3:c.3253C>T | XP_006717693.1:p.Leu1085Phe | |
| XR_945604.3:n.4192C>T | ||
| XR_945605.3:n.4065C>T |