MyVariant.info:
GRCh37
chr16:g.14041526T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13947669T>C , CM000678.2:g.13947669T>C | GRCh38 |
| NC_000016.9:g.14041526T>C , CM000678.1:g.14041526T>C | GRCh37 |
| NC_000016.8:g.13949027T>C | NCBI36 |
| NG_011442.1:g.32513T>C , LRG_463:g.32513T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2211T>C | ENSP00000507912.1:p.Phe737= | |
| ENST00000683962.1:c.*1767T>C | ENSP00000506854.1:n.*1767T>C | |
| ENST00000311895.8:c.2073T>C MANE Select | ENSP00000310520.7:p.Phe691= | |
| ENST00000311895.7:c.2073T>C | ENSP00000310520.7:p.Phe691= | |
| ENST00000389138.7:n.1350T>C | ||
| ENST00000462862.1:c.386T>C | ENSP00000461322.1:n.386T>C | |
| NM_005236.2:c.2073T>C , LRG_463t1:c.2073T>C | NP_005227.1:p.Phe691= | |
| XM_011522424.1:c.2211T>C | XP_011520726.1:p.Phe737= | |
| XM_011522425.1:c.1530T>C | XP_011520727.1:p.Phe510= | |
| XM_011522426.1:c.1284T>C | XP_011520728.1:p.Phe428= | |
| XM_011522427.1:c.723T>C | XP_011520729.1:p.Phe241= | |
| XR_932805.1:n.2232T>C | ||
| XM_011522424.3:c.2211T>C | XP_011520726.1:p.Phe737= | |
| XM_017023043.2:c.1284T>C | XP_016878532.1:p.Phe428= | |
| NM_005236.3:c.2073T>C MANE Select | NP_005227.1:p.Phe691= |